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Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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SKU | Size | Availability | Price | Qty |
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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 |
Synonyms | SCHEMBL340780 | 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 |
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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. |
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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IUPAC Name | N-phenylethanethioamide |
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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 |
Enter Lot Number to search for COA:
Find and download the COA for your product by matching the lot number on the packaging.
Lot Number | Certificate Type | Date | Item |
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H1926176 | Certificate of Analysis | Jun 07, 2023 | T161816 |
Boil Point(°C) | 147°C/1mmHg |
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Melt Point(°C) | 76-79°C |
Hazard Statements | H312+H332:Harmful in contact with skin or if inhaled |
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Precautionary Statements | P280:Wear protective gloves/protective clothing/eye protection/face protection. |
WGK Germany | 3 |
RTECS | AE7350000 |
Reaxy-Rn | 2205727 |
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] |