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Thioacetanilide - >98.0%, high purity , CAS No.637-53-6

≥98%

CAS#: 637-53-6
Formula: C₈H₉NS
Molecular Weight: 151.23
Beilstein Registry Number: 12245
MDL number: MFCD00004942
PubChem CID: 820777

Item Number

T161816

Grouped product items
SKU	Size	Availability	Price	Qty
T161816-1g	1g	In stock	$63.90
T161816-5g	5g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$244.90

View related series

Non heterocyclic block Sulfur containing compounds

Basic Description

Synonyms	Thioacetanilide \| 637-53-6 \| N-Phenylethanethioamide \| Ethanethioamide, N-phenyl- \| ACETANILIDE, THIO- \| N-Phenylthioacetamide \| USAF EK-1902 \| L9AL2GO03Y \| CHEMBL3740596 \| NSC-36984 \| EINECS 211-288-4 \| NSC 36984 \| UNII-L9AL2GO03Y \| BRN 2205727 \| AI3-00235 \| N-Phenyl-thioacetamide \| Th
Specifications & Purity	≥98%
Shipped In	Normal
Note	5G卖完停产，不再备货
Product Description	Metabolism and acute toxicity of thioacetanilide has been studied in rat. Thioacetanilide undergoes nucleophilic addition reaction with superoxide ion in dimethyl sulfoxide.

Associated Targets(Human)

TYR Tclin Tyrosinase (717 Activities)

Discover Target: TYR

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

TAS2R38 Tchem Taste receptor type 2 member 38 (37 Activities)

Discover Target: TAS2R38

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

Names and Identifiers

IUPAC Name	N-phenylethanethioamide
INCHI	InChI=1S/C8H9NS/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10)
InChi Key	MWCGLTCRJJFXKR-UHFFFAOYSA-N
Canonical SMILES	CC(=S)NC1=CC=CC=C1
Isomeric SMILES	CC(=S)NC1=CC=CC=C1
WGK Germany	3
RTECS	AE7350000
PubChem CID	820777
Molecular Weight	151.23
Beilstein	12245
Reaxy-Rn	2205727

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Certificate of Analysis(COA)

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Lot Number	Certificate Type	Date	Item
H1926176	Certificate of Analysis	Jun 07, 2023	T161816

Boil Point(°C)

147°C/1mmHg

Melt Point(°C)

76-79°C

Hazard Statements

H312+H332:Harmful in contact with skin or if inhaled

Precautionary Statements

P280:Wear protective gloves/protective clothing/eye protection/face protection.

WGK Germany

RTECS

AE7350000

Reaxy-Rn

2205727

References

1. Toshiyuki Kitai,Toshihiro Nishio,Mitsuharu Miwa,Yoshio Yamaoka. (2004-04-27) Optical analysis of the cirrhotic liver by near-infrared time-resolved spectroscopy.. Surgery today, 34 ((5)): (424-428). [PMID:15108081]
2. Ester Muraglia,Olaf D Kinzel,Ralph Laufer,Michael D Miller,Gregory Moyer,Vandna Munshi,Federica Orvieto,Maria Cecilia Palumbi,Giovanna Pescatore,Michael Rowley,Peter D Williams,Vincenzo Summa. (2006-03-01) Tetrazole thioacetanilides: potent non-nucleoside inhibitors of WT HIV reverse transcriptase and its K103N mutant.. Bioorganic & medicinal chemistry letters, 16 ((10)): (2748-2752). [PMID:16503141]
3. Peng Zhan,Xinyong Liu,Junjie Zhu,Zengjun Fang,Zhenyu Li,Christophe Pannecouque,Erik De Clercq. (2009-08-01) Synthesis and biological evaluation of imidazole thioacetanilides as novel non-nucleoside HIV-1 reverse transcriptase inhibitors.. Bioorganic & medicinal chemistry, 17 ((16)): (5775-5781). [PMID:19643613]
4. Peng Zhan,Xinyong Liu,Zengjun Fang,Christophe Pannecouque,Erik De Clercq. (2009-08-04) 1,2,3-Selenadiazole thioacetanilides: synthesis and anti-HIV activity evaluation.. Bioorganic & medicinal chemistry, 17 ((17)): (6374-6379). [PMID:19647440]
5. P N Trennery,R H Waring. (1983-08-01) The metabolism of thioacetanilide in the rat.. Xenobiotica; the fate of foreign compounds in biological systems, 13 ((8)): (475-482). [PMID:6649681]
6. Li-Rong Wen,Ji-Hui Sun,Ming Li,En-Tao Sun,Shu-Sheng Zhang. (2008-01-29) Application of beta-(2-chloroaroyl) thioacetanilides in synthesis: an unusual and highly efficient access to thiochromeno[2,3-b]pyridine derivatives.. The Journal of organic chemistry, 73 ((5)): (1852-1863). [PMID:18220410]
7. Anna Michta,Elzbieta Chełmecka,Maria Nowak,Joachim Kusz. (2008-08-07) Thioacetanilide at 120 K.. Acta crystallographica. Section C, Crystal structure communications, 64 ((Pt 8)): (o411-o413). [PMID:18682643]
8. Xiao Li,Peng Zhan,Hong Liu,Dongyue Li,Liu Wang,Xuwang Chen,Huiqing Liu,Christophe Pannecouque,Jan Balzarini,Erik De Clercq,Xinyong Liu. (2012-08-14) Arylazolyl(azinyl)thioacetanilides. Part 10: design, synthesis and biological evaluation of novel substituted imidazopyridinylthioacetanilides as potent HIV-1 inhibitors.. Bioorganic & medicinal chemistry, 20 ((18)): (5527-5536). [PMID:22883027]

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