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

  • ≥98%
Item Number
T161816
Grouped product items
SKUSizeAvailabilityPrice 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

Basic Description

SynonymsSCHEMBL340780 | WLN: SUY1&MR | FT-0693782 | BDBM50499816 | CS-0107756 | MFCD00004942 | EINECS 211-288-4 | BRN 2205727 | Q27282872 | THIOACETANILIDE [INCI] | Thioacetanilide, 98% | NSC36984 | NSC-36984 | AQ-012/40221353 | Ethanethioamide, N-phenyl- | Thioa
Specifications & Purity≥98%
Shipped InNormal
Note5G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)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

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

Certificates

Certificate of Analysis(COA)

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Lot NumberCertificate TypeDateItem
H1926176Certificate of AnalysisJun 07, 2023 T161816

Chemical and Physical Properties

Boil Point(°C)147°C/1mmHg
Melt Point(°C)76-79°C

Safety and Hazards(GHS)

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 3
RTECS AE7350000
Reaxy-Rn 2205727

Related Documents

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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