91133-15-2

Basic information

• Product Name: N-(2-Mercaptoethyl)-acetamide benzoate
• Synonyms: N-(2-Mercaptoethyl)-acetamide benzoate
• CAS NO: 91133-15-2
• Molecular Formula: C₁₁H₁₃NO₂S
• Molecular Weight: 241.3067
• Mol File: 91133-15-2.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 410.8°C at 760 mmHg
• Flash Point: 202.3°C
• Appearance: /
• Density: 1.172g/cm³
• Vapor Pressure: 5.85E-07mmHg at 25°C
• Refractive Index: 1.562
• CAS DataBase Reference: N-(2-Mercaptoethyl)-acetamide benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-Mercaptoethyl)-acetamide benzoate(91133-15-2)
• EPA Substance Registry System: N-(2-Mercaptoethyl)-acetamide benzoate(91133-15-2)

Safety Data

• Hazardous Substances Data: 91133-15-2(Hazardous Substances Data)

Usage

General Description

N-(2-Mercaptoethyl)-acetamide benzoate is a chemical compound that is derived from acetamide and benzoate. It is composed of a benzene ring with a carboxylic acid group and an amino group, as well as a thiol group connected to an ethyl chain. N-(2-Mercaptoethyl)-acetamide benzoate has potential uses in pharmaceuticals as a chelating agent for metal ions and as a potential protective agent against oxidative stress. Additionally, it may have applications in the synthesis of organic compounds due to its thiol and amide functional groups. However, further research is needed to fully understand the potential uses and properties of N-(2-Mercaptoethyl)-acetamide benzoate.

InChI:InChI=1/C11H13NO2S/c1-9(13)12-7-8-15-11(14)10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,12,13)

Upstream product

• 1190-73-4 2-(acetylamino)ethanethiol 
• 98-88-4 benzoyl chloride 
• 2722-34-1 2-phenylthiazoline 
• 108-24-7 acetic anhydride 
• 65-85-0 benzoic acid 

Downstream Products

• 20851-38-1 4-hydroxy-6-(2-oxo-2-phenylethyl)-2H-pyran-2-one 
• 5526-38-5 4-hydroxy-6-phenyl-2H-pyran-2-one 
• 1443502-35-9 urauchimycin B 

Relevant articles and documents

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The in vivo and in vitro characterization of AntB, a dedicated acyltransferase encoded in the antimycin biosynthetic gene cluster, which catalyzes the C-8 acyloxy formation is reported. It is demonstrated that AntB has broad substrate specificity toward both the acyl substrate and the acyl carrier and produces more antimycin analogues with varying C-8 acyloxy moieties.

Unnatural polyketide analogues selectively target the her signaling pathway in human breast cancer cells

Receptor tyrosine kinases are critical targets for the regulation of cell survival. Cancer patients with abnormal receptor tyrosine kinases (RTK) tend to have more aggressive disease with poor clinical outcomes. As a result, human epidermal growth factor

Antiparasitic agents

Antiparasitic compound of formula (I): STR1 The broken line at the 22-23 position representing an optional double bond and either R1 is a H or OH and the double bond is absent or the double bond is present and R1 is absent; R2 is optionally substituted phenyl, or a group of formula (II): STR2 wherein X is O, S or --CH2 --, abc and d are 0-2 and a+b+c+d≤5 R3 is H or Me R4 is H, OH or 4'-(alpha-L-oleandrosyl)-alpha-L-oleandrosyloxy. The compounds are prepared by fermentation of Streptomyces avermitilis in the presence of an N-alkanoyl cysteamine thioester containing R2.