1153277-69-0

Basic information

• Product Name: 3-[(4-acetylphenyl)thio]-propanoic acid methyl ester
• Synonyms: 3-[(4-acetylphenyl)thio]-propanoic acid methyl ester
• CAS NO: 1153277-69-0
• Molecular Weight: 238.307
• Mol File: 1153277-69-0.mol

Chemical Properties

• CAS DataBase Reference: 3-[(4-acetylphenyl)thio]-propanoic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[(4-acetylphenyl)thio]-propanoic acid methyl ester(1153277-69-0)
• EPA Substance Registry System: 3-[(4-acetylphenyl)thio]-propanoic acid methyl ester(1153277-69-0)

Safety Data

• Hazardous Substances Data: 1153277-69-0(Hazardous Substances Data)

Upstream product

• 3814-20-8 4-mercaptoacetophenone 
• 292638-85-8 acrylic acid methyl ester 
• 2935-90-2 Methyl 3-mercaptopropionate 
• 99-90-1 para-bromoacetophenone 

Downstream Products

• 1335144-55-2 5,10,15,20,22,24-hexahydro-5,5,10,15,15,20-hexamethyl-10α,20β-bis[4-(2-methoxycarbonylethyl-1-sulfonyl)phenyl]-calix[4]pyrrole 
• 1335144-52-9 5,10,15,20,22,24-hexahydro-5,5,10,15,15,20-hexamethyl-10α,20α-bis[4-(2-methoxycarbonylethyl-1-sulfonyl)phenyl]-calix[4]pyrrole 
• 1335144-54-1 5,10,15,20,22,24-hexahydro-5,5,10,15,15,20-hexamethyl-10α-[4-(2-methoxycarbonylethyl-1-sulfonyl)phenyl]-20β-[4-(2-methoxycarbonylethyl-1-thio)phenyl]-calix[4]pyrrole 
• 1335144-50-7 5,10,15,20,22,24-hexahydro-5,5,10,15,15,20-hexamethyl-10α-[4-(2-methoxycarbonylethyl-1-sulfonyl)phenyl]-20α-[4-(2-methoxycarbonylethyl-1-thio)phenyl]-calix[4]pyrrole 
• 1335144-53-0 5,10,15,20,22,24-hexahydro-5,5,10,15,15,20-hexamethyl-10α,20β-bis-[4-(2-methoxycarbonylethyl-1-thio)phenyl]-calix[4]pyrrole 
• 1335144-49-4 5,10,15,20,22,24-hexahydro-5,5,10,15,15,20-hexamethyl-10α,20α-bis-[4-(2-methoxycarbonylethyl-1-thio)phenyl]-calix[4]pyrrole 
• 1335144-48-3 5-methyl-5-[4-(2-methoxycarbonylethyl-1-sulfonyl)phenyl]dipyrromethane 
• 1335144-47-2 5-methyl-5-[4-(2-methoxycarbonylethyl-1-thio)phenyl]dipyrromethane 

Relevant articles and documents

A Strategy for the Synthesis of Sulfonamides on DNA

An efficient method is reported to synthesize sulfonamides on DNA from sulfinic acids or sodium sulfinates and amines in the presence of iodine under mild conditions. This method demonstrates a major expansion of scope of sulfonamide formation on DNA through the utilization of a novel sodium carbonate-sodium sulfinate bifunctional reagent class.

Synthesis and structural features of sulfur-substituted calix[4]pyrrole for a bottom-up control of the substrate-directed self-assembly of supramolecular structures

The synthesis of six new calix[4]pyrroles, containing sulfur-substituted phenylene units is reported. Halogen-anions and organic aromatic mono- and bis-anions have been selected to explore the formation of host-guest complexes and the possible self-assembly of multi-component structures with the six calixpyrroles. The type of aryl substitution modulates the strength of binding and the selectivity towards different anions and, in some cases, the combination of receptors and bis-anionic precursors, offers a way to build systems in which capsular assemblies are observed.