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2-Aminothiazole - 97%, high purity , CAS No.96-50-4

≥97%

CAS#: 96-50-4
Formula: C₃H₄N₂S
Molecular Weight: 100.14
Beilstein Registry Number: 105738
EC Number: 202-511-6
MDL number: MFCD00005325
PubChem CID: 2155
PubChem SID: 488179668

Item Number

A104872

Grouped product items
SKU	Size	Availability	Price
A104872-25g	25g	In stock	$19.90
A104872-100g	100g	In stock	$71.90
A104872-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$323.90

View related series

Five-Membered Heterocyclic Compounds Thiazoles

Basic Description

Synonyms	2-AMINOTHIAZOLE \| aminothiazole \| 96-50-4 \| thiazol-2-amine \| 2-Thiazolamine \| 1,3-Thiazol-2-amine \| 2-Thiazolylamine \| Abadole \| Abadol \| Basedol \| 2-Thiazylamine \| 4-Thiazolin-2-onimine \| Thiazolamine \| 2-Amino-1,3-thiazole \| 2-Aminothiazol \| Aminothiazol \| Aminothiazolum \| Aminotiazol \|
Specifications & Purity	≥97%
Biochemical and Physiological Mechanisms	2-Aminothiazole is a potent cyclin-dependent kinase 5 inhibitor and is a therapeutic drug for Alzheimer's disease and other neurodegenerative diseases.
Storage Temp	Protected from light,Argon charged
Shipped In	Normal
Product Description	Usually used in the synthesis of 2-aminothiazole-modified silica gel，and aslo used in Ulmann coupling with 2-chlorobenzoic acids mediated by ultrasonic irradiation.

Associated Targets(Human)

HSD17B10 Tchem 3-hydroxyacyl-CoA dehydrogenase type-2 0 Activities

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

HDAC6 Tclin Histone deacetylase 6 0 Activities

Discover Target: HDAC6

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 0 Activities

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 0 Activities

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

TSHR Tclin Thyrotropin receptor 0 Activities

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

MAOB Tclin Amine oxidase [flavin-containing] B 0 Activities

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

MAOA Tclin Amine oxidase [flavin-containing] A 0 Activities

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

ALDH1A1 Tchem Retinal dehydrogenase 1 0 Activities

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PRKAA2 Tchem 5'-AMP-activated protein kinase catalytic subunit alpha-2 0 Activities

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

GLS Tchem Glutaminase kidney isoform, mitochondrial 0 Activities

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Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

NOS2 Tchem Nitric oxide synthase, inducible 0 Activities

Discover Target: NOS2

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

NOS1 Tchem Nitric oxide synthase, brain 0 Activities

Discover Target: NOS1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Thyroid stimulating hormone receptor 29986 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Monoamine oxidase A 11911 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Monoamine oxidase B 8835 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

AMP-activated protein kinase, alpha-2 subunit 1328 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Nitric-oxide synthase, brain 1786 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Aldehyde dehydrogenase 1A1 77053 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Endoplasmic reticulum-associated amyloid beta-peptide-binding protein 20669 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Solute carrier organic anion transporter family member 1B1 2672 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Solute carrier organic anion transporter family member 1B3 2517 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Glutaminase kidney isoform, mitochondrial 16997 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

D-alanylalanine synthetase 66 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

UDP-N-acetylglucosamine 1-carboxyvinyltransferase 389 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Nitric oxide synthase, inducible 3573 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Histone deacetylase 6 222 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Salmonella typhimurium 15756 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Plasmodium falciparum 966862 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cavia porcellus 23802 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Replicase polyprotein 1ab 378 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Plasma 328 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

SARS-CoV-2 38078 Activities

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Names and Identifiers

Pubchem Sid	488179668
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488179668
IUPAC Name	1,3-thiazol-2-amine
INCHI	InChI=1S/C3H4N2S/c4-3-5-1-2-6-3/h1-2H,(H2,4,5)
InChi Key	RAIPHJJURHTUIC-UHFFFAOYSA-N
Canonical SMILES	C1=CSC(=N1)N
Isomeric SMILES	C1=CSC(=N1)N
WGK Germany	3
RTECS	XJ2100000
PubChem CID	2155
Molecular Weight	100.14
Beilstein	105738
Reaxy-Rn	105738

Certificates

Certificate of Analysis(COA)

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17 results found

Lot Number	Certificate Type	Date	Item
D2013124	Certificate of Analysis	Jan 30, 2024	A104872
G1527002	Certificate of Analysis	Mar 08, 2023	A104872
B2322249	Certificate of Analysis	Feb 25, 2023	A104872
H2318182	Certificate of Analysis	Feb 15, 2023	A104872
H2318183	Certificate of Analysis	Feb 15, 2023	A104872
H2318184	Certificate of Analysis	Feb 15, 2023	A104872
H2318186	Certificate of Analysis	Feb 15, 2023	A104872
I1827030	Certificate of Analysis	Aug 06, 2022	A104872
H2201067	Certificate of Analysis	Aug 04, 2022	A104872
J2220106	Certificate of Analysis	Jul 26, 2022	A104872
J2220103	Certificate of Analysis	Jul 26, 2022	A104872
J2220094	Certificate of Analysis	Jul 26, 2022	A104872
J2220093	Certificate of Analysis	Jul 26, 2022	A104872
B2322295	Certificate of Analysis	Jul 26, 2022	A104872
F2223102	Certificate of Analysis	Jun 25, 2022	A104872
F2222470	Certificate of Analysis	Jun 25, 2022	A104872
C1802027	Certificate of Analysis	Jan 18, 2022	A104872

Chemical and Physical Properties

Solubility	Soluble in water, alcohol and ether
Sensitivity	Light Sensitive,Air Sensitive
Boil Point(°C)	117°C
Melt Point(°C)	93°C

Safety and Hazards(GHS)

Pictogram(s)	GHS07
Signal	Warning
Hazard Statements	H319:Causes serious eye irritation H302:Harmful if swallowed
Precautionary Statements	P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing. P280:Wear protective gloves/protective clothing/eye protection/face protection. P501:Dispose of contents/container to ... P264:Wash hands [and …] thoroughly after handling. P270:Do not eat, drink or smoke when using this product. P330:Rinse mouth. P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes. P301+P317:IF SWALLOWED: Get medical help. P337+P317:If eye irritation persists: Get medical help.
WGK Germany	3
RTECS	XJ2100000
Reaxy-Rn	105738
Merck Index	479

FAQs and Articles

FAQ

1,3-Thiazole building blocks in natural products and synthetic materials

Categories: Technical articles

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1,3-Thiazole building blocks

Citations of This Product

1. Pei Chen, Hui Zhu, Tianhao Na, Yong Yi, Jian Zhou, Tao Duan, Jiehong Lei. (2023) Functionalized collagen fiber with specific recognition sites for highly efficient iodine capture: theoretical calculations and experimental verification. CHEMICAL ENGINEERING JOURNAL, 476 (15): (146660). [PMID:12432077]
2. Jiahui Xu, Jia-qi Bai, Wenjie Si, Yunhai Zhang, Jiazhao Tan, Mengdie Cai, Qin Cheng, Song Sun. (2023) N,S-Co-doping Significantly Improves the Co–Nx Content of the Co-NSPC Catalyst and Enhances the Catalytic Performance for Selective Hydrogenation of Halogenated Nitrobenzenes. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 62 (9): (3862–3872). [PMID:]
3. Xiaoyun Zhang, Yinhang Zhang, Yuxin Su, Xiaoyang Wang, Renqing Lv. (2022) Synthesis and Corrosion Inhibition Performance of Mannich Bases on Mild Steel in Lactic Acid Media. ACS Omega, 7 (36): (32208–32224). [PMID:36120014]

References

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10. Meredeth A McGowan,Jaclyn L Henderson,Stephen L Buchwald. (2012-03-08) Palladium-catalyzed N-arylation of 2-aminothiazoles.. Organic letters, 14 ((6)): (1432-1435). [PMID:22394197]
11. Breland Smith,Hui-Hua Chang,Federico Medda,Vijay Gokhale,Justin Dietrich,Angela Davis,Emmanuelle J Meuillet,Christopher Hulme. (2012-04-21) Synthesis and biological activity of 2-aminothiazoles as novel inhibitors of PGE2 production in cells.. Bioorganic & medicinal chemistry letters, 22 ((10)): (3567-3570). [PMID:22516282]
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13. Sivakumar Annadurai,Rogelio Martinez,Daniel J Canney,Tess Eidem,Paul M Dunman,Magid Abou-Gharbia. (2012-11-03) Design and synthesis of 2-aminothiazole based antimicrobials targeting MRSA.. Bioorganic & medicinal chemistry letters, 22 ((24)): (7719-7725). [PMID:23116888]
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15. B Michael Silber,Satish Rao,Kimberly L Fife,Alejandra Gallardo-Godoy,Adam R Renslo,Deepak K Dalvie,Kurt Giles,Yevgeniy Freyman,Manuel Elepano,Joel R Gever,Zhe Li,Matthew P Jacobson,Yong Huang,Leslie Z Benet,Stanley B Prusiner. (2013-02-19) Pharmacokinetics and metabolism of 2-aminothiazoles with antiprion activity in mice.. Pharmaceutical research, 30 ((4)): (932-950). [PMID:23417511]
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17. Naoki Aizawa,Yukio Homma,Yasuhiko Igawa. (2014-02-18) Effects of L-arginine, mirabegron, and oxybutynin on the primary bladder afferent nerve activities synchronized with reflexic, rhythmic bladder contractions in the rat.. Neurourology and urodynamics, 34 ((4)): (368-374). [PMID:24532414]
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21. Xin Cao,Qi-Dong You,Zhi-Yu Li,Qing-Long Guo,Jing Shang,Ming Yan,Ji-Wang Chern,Men-Ling Chen. (2008-05-20) Design and synthesis of 7-alkoxy-4-heteroarylamino-3-quinolinecarbonitriles as dual inhibitors of c-Src kinase and nitric oxide synthase.. Bioorganic & medicinal chemistry, 16 ((11)): (5890-5898). [PMID:18485715]
22. Mari Kuramoto,Yoko Sakata,Kumi Terai,Ikuo Kawasaki,Jun-Ichi Kunitomo,Takahiro Ohishi,Takehiko Yokomizo,Seiichi Takeda,Shuichi Tanaka,Yoshitaka Ohishi. (2008-07-18) Preparation of leukotriene B(4) inhibitory active 2- and 3-(2-aminothiazol-4-yl)benzo[b]furan derivatives and their growth inhibitory activity on human pancreatic cancer cells.. Organic & biomolecular chemistry, 6 ((15)): (2772-2781). [PMID:18633535]
23. Xin Cao,Qi-Dong You,Zhi-Yu Li,Xiao-Rong Liu,Dan Xu,Qing-Long Guo,Jing Shang,Ji-Wang Chern,Meng-Ling Chen. (2008-10-22) The design, synthesis and biological evaluation of 7-alkoxy-4-heteroarylamino-3-cyanoquinolines as dual inhibitors of c-Src and iNOS.. Bioorganic & medicinal chemistry letters, 18 ((23)): (6206-6209). [PMID:18930653]
24. Jiazhong Li,Juan Du,Lili Xi,Huanxiang Liu,Xiaojun Yao,Mancang Liu. (2008-12-03) Validated quantitative structure-activity relationship analysis of a series of 2-aminothiazole based p56(Lck) inhibitors.. Analytica chimica acta, 631 ((1)): (29-39). [PMID:19046675]
25. Sina Ghaemmaghami,Barnaby C H May,Adam R Renslo,Stanley B Prusiner. (2009-12-25) Discovery of 2-aminothiazoles as potent antiprion compounds.. Journal of virology, 84 ((7)): (3408-3412). [PMID:20032192]
26. R Romagnoli,P G Baraldi,M A Tabrizi,S Gessi,P A Borea,S Merighi. (2010-08-27) Allosteric enhancers of A1 adenosine receptors: state of the art and new horizons for drug development.. Current medicinal chemistry, 17 ((30)): (3488-3502). [PMID:20738250]
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28. M Kalanithi,D Kodimunthiri,M Rajarajan,P Tharmaraj. (2011-08-10) Synthesis, characterization and biological activity of some new VO(IV), Co(II), Ni(II), Cu(II) and Zn(II) complexes of chromone based NNO Schiff base derived from 2-aminothiazole.. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 82 ((1)): (290-298). [PMID:21824811]
29. Mattia Mori,Cristina Tintori,Robert Selwyne Arul Christopher,Marco Radi,Silvia Schenone,Francesca Musumeci,Chiara Brullo,Patrizia Sanità,Simona Delle Monache,Adriano Angelucci,Miroslava Kissova,Emmanuele Crespan,Giovanni Maga,Maurizio Botta. (2013-02-26) A combination strategy to inhibit Pim-1: synergism between noncompetitive and ATP-competitive inhibitors.. ChemMedChem, 8 ((3)): (484-496). [PMID:23436791]
30. Xi-Zhi Niu,Julie Glady-Croué,Jean-Philippe Croué. (2017-08-16) Photodegradation of sulfathiazole under simulated sunlight: Kinetics, photo-induced structural rearrangement, and antimicrobial activities of photoproducts.. Water research, 124 (576-583). [PMID:28810229]
31. Pei Chen, Hui Zhu, Tianhao Na, Yong Yi, Jian Zhou, Tao Duan, Jiehong Lei. (2023) Functionalized collagen fiber with specific recognition sites for highly efficient iodine capture: theoretical calculations and experimental verification. CHEMICAL ENGINEERING JOURNAL, 476 (15): (146660). [PMID:12432077]
32. Jiahui Xu, Jia-qi Bai, Wenjie Si, Yunhai Zhang, Jiazhao Tan, Mengdie Cai, Qin Cheng, Song Sun. (2023) N,S-Co-doping Significantly Improves the Co–Nx Content of the Co-NSPC Catalyst and Enhances the Catalytic Performance for Selective Hydrogenation of Halogenated Nitrobenzenes. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 62 (9): (3862–3872). [PMID:]
33. Xiaoyun Zhang, Yinhang Zhang, Yuxin Su, Xiaoyang Wang, Renqing Lv. (2022) Synthesis and Corrosion Inhibition Performance of Mannich Bases on Mild Steel in Lactic Acid Media. ACS Omega, 7 (36): (32208–32224). [PMID:36120014]

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