88999-93-3

Basic information

• Product Name: 3-(4-bromphenyl)propane-1-thiol
• Synonyms: 3-(4-bromphenyl)propane-1-thiol
• CAS NO: 88999-93-3
• Molecular Weight: 231.156
• Mol File: 88999-93-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-(4-bromphenyl)propane-1-thiol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-bromphenyl)propane-1-thiol(88999-93-3)
• EPA Substance Registry System: 3-(4-bromphenyl)propane-1-thiol(88999-93-3)

Safety Data

• Hazardous Substances Data: 88999-93-3(Hazardous Substances Data)

Upstream product

• 74003-34-2 1-bromo-4-(3-chloropropyl)benzene 
• 90562-10-0 trans-1-(3-bromopropyl)-4-bromobenzene 
• 25574-11-2 3-(4-bromophenyl)propanol 
• 362529-44-0 S-3-(4-bromophenyl)propyl thioacetate 
• 35656-89-4 4-(4-bromophenyl)butanoic acid 

Downstream Products

• 1238799-77-3 3-(4-bromophenyl)propyl-1-S-triisopropylsilyl sulfide 

Relevant articles and documents

Mo-Based Oxidizers as Powerful Tools for the Synthesis of Thia- and Selenaheterocycles

A highly efficient synthetic protocol for the synthesis of thia- and selenaheterocycles has been developed. By employing a MoCl5-mediated intramolecular dehydrogenative coupling reaction, a broad variety of structural motifs was isolated in yields up to 94 %. The electrophilic key transformation is tolerated by several labile moieties like halides and tertiary alkyl groups. Due to the use of disulfide or diselenide precursors, a high atom efficiency was achieved.

Uracil derivatives. IV. Growth-inhibitory activity against L-1210 cells of orotic acid derivatives and synthesis of 1-(β-D-ribofuranosyl)furo[3,4-d]pyrimidine-2,4,7(1H,3H,5H)-trione

5-(Substituted thiomethyl)-6-carbamoyluracils (IIIb-h) and 5-(substituted thiomethyl)-uracils (Va-h) were prepared and their ability to inhibit the growth of L-1210 cells in vitro was examined. The reaction of silylated furo[3,4-d]pyrimidine-2,4,7(1H,3H,5