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

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

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.

A divergent synthesis of oligoarylalkanethiols with Lewis-basic N-donor termini

Araliphatic thiols are key molecules for the formation of self-assembled monolayers with high long-range order. If these monolayers shall act as bases for the attachment of other molecules, the respective thiols need to carry suitable functional groups, such as the amino or the pyridine group. Due to their Lewis-basicity, these groups are not compatible with the thiol group under most reaction conditions. Here, an entry into this versatile class of compounds is presented, by using fundamental building blocks in which the thiol groups are protected as triisopropylsilyl sulfides making them compatible with many reagents including Grignard reagents and palladium catalysts. With this strategy at hand, six thiols with bi- and terphenyl backbones, one to three methylene groups, and amino or pyridine head groups became accessible in short reaction sequences. The Royal Society of Chemistry 2010.

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