17742-50-6

Basic information

• Product Name: Acetic acid, [[(4-bromophenyl)methyl]thio]-
• CAS NO: 17742-50-6
• Molecular Formula: C9H9BrO2S
• Molecular Weight: 261.139
• Mol File: 17742-50-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Acetic acid, [[(4-bromophenyl)methyl]thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid, [[(4-bromophenyl)methyl]thio]-(17742-50-6)
• EPA Substance Registry System: Acetic acid, [[(4-bromophenyl)methyl]thio]-(17742-50-6)

Safety Data

• Hazardous Substances Data: 17742-50-6(Hazardous Substances Data)

Upstream product

• 19552-10-4 4-bromobenzyl mercaptan 
• 79-08-3 bromoacetic acid 
• 106-38-7 para-bromotoluene 
• 68-11-1 mercaptoacetic acid 
• 589-15-1 1-bromomethyl-4-bromobenzene 

Downstream Products

• 1449109-74-3 BrC₆H₄CH₂SCH₂C(O)Cl 
• 15909-40-7 N--hydroxylamin 
• 81431-45-0 2-[(4-bromobenzyl)sulfonyl]acetic acid 
• 669726-55-0 (4-Bromo-benzylsulfanyl)-acetic acid methyl ester 

Relevant articles and documents

Design, synthesis and evaluation of 3-substituted coumarin derivatives as anti-inflammatory agents

Coumarin moiety has garnered momentous attention especially in the design of compounds with significant biological activities. In this work, a series of 3-substituted coumarin derivatives 6a-6l were synthesized and fully characterized. Most of the compoun

Synthesis of some sulfur-containing acylferrocenes

Acylferrocenes containing a sulfur atom within their side chain were synthesized in good yields by Friedel-Crafts acylation of ferrocene with in situ generated acyl halides from the corresponding carboxylic acids (S-protected derivatives of thioglicolic and α- and β-mercaptopropionic acids).

EFFECT OF MOLECULAR STRUCTURE ON OPTICAL PROPERTIES OF SULFOXIDE SYSTEMS. p-BROMOBENZYLSULFINYLACETIC ACIDS AND SOME OF THEIR DERIVATIVES. PART III

The synthesis and principal properties of p-bromobenzylsulfinylacetic and p-bromobenzylsulfonylacetic acids are described.Racemic sulfoxide was resolved by crystallization of its diastereomeric salts with optically active bases.The relative configuration of the enantiomers were elucidated.Optical rotatory dispersion of the dextrorotatory enantiomers, its ester and amide in the region 340, ΔH) of racemization of laevorotatory p-bromobenzylsulfinylacetic acid were determined by the classical kinetic methods.