
CAS 588-07-8: N-(3-Chlorophenyl)acetamide
Formula:C8H8ClNO
InChI:InChI=1S/C8H8ClNO/c1-6(11)10-8-4-2-3-7(9)5-8/h2-5H,1H3,(H,10,11)
InChI key:InChIKey=MUUQHCOAOLLHIL-UHFFFAOYSA-N
SMILES:N(C(C)=O)C1=CC(Cl)=CC=C1
Synonyms:- Acetamide, N-(3-chlorophenyl)-
- Acetanilide, 3'-chloro-
- Acetic acid, amide, N(3-chlorophenyl)-
- Brn 2208105
- Hsdb 1409
- N-(3-Chlorophenyl)acetamide
- Nsc 39967
- Nsc 6116
- m-Chloroacetanilide
- meta-Chloroacetanilide
- 3-Chloroacetanilide
- See more synonyms
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Found 5 products.
3'-Chloroacetanilide
CAS:Formula:C8H8ClNOPurity:>98.0%(GC)Color and Shape:White to Light red to Green powder to crystalMolecular weight:169.613'-Chloroacetanilide
CAS:3'-Chloroacetanilide is a chemical compound that has been shown to inhibit the acetylation of adenosine nucleotides in vitro, leading to an increase in ATP levels. 3'-Chloroacetanilide also inhibits the deamination of guanosine nucleotides and blocks the synthesis of purines. The molecular modeling studies of this chemical have shown that it could be a potential inhibitor for cancer cells. In vivo experiments have shown that 3'-chloroacetanilide can cause a decrease in tumor size and weight as well as an increase in apoptosis. When incubated with rat hepatocytes, 3'-chloroacetanilide caused a significant drop in ATP levels and an increase in AMP levels. This study also showed that 3'-chloroacetanilide is metabolized into its glucuronide conjugate, which is excreted by the kidneys.br>br> br> 3'-ChlorFormula:C8H8ClNOPurity:Min. 95%Molecular weight:169.61 g/mol3-Chloroacetanilide
CAS:Controlled ProductApplications 3-Chloroacetanilide is a major metabolite of chlorpropham. An acetanilide herbicide derivative. References Carrera, G., et al.: Arch. Environ. Cont. Tox., 35, 89 (1998); Freitas, M. R., et al.: Bull. Environ. Contam. Toxicol., 92, 143 (2014)Formula:C8H8ClNOColor and Shape:NeatMolecular weight:169.608