147227-33-6

Basic information

• Product Name: Pyrrolidine, 1-[(4-bromophenyl)azo]-
• CAS NO: 147227-33-6
• Molecular Formula: C10H12BrN3
• Molecular Weight: 254.129
• Mol File: 147227-33-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Pyrrolidine, 1-[(4-bromophenyl)azo]-(CAS DataBase Reference)
• NIST Chemistry Reference: Pyrrolidine, 1-[(4-bromophenyl)azo]-(147227-33-6)
• EPA Substance Registry System: Pyrrolidine, 1-[(4-bromophenyl)azo]-(147227-33-6)

Safety Data

• Hazardous Substances Data: 147227-33-6(Hazardous Substances Data)

Upstream product

• 123-75-1 pyrrolidine 
• 106-40-1 4-bromo-aniline 

Downstream Products

• 1111735-05-7 3-(4-aminophenyl)oxetan-3-ol 
• 1259224-11-7 5-bromo-2,3-diphenyl-1H-indole 
• 53136-21-3 1-benzylsulphanyl-4-bromobenzene 
• 68716-49-4 p-bromophenylboronic acid pinacol ester 
• 92-66-0 4-bromo-1,1'-biphenyl 
• 196599-46-9 1-[2-(4-ethynylphenyl)diazenyl]pyrrolidine 
• 58743-83-2 4-bromo-4'-methoxylbiphenyl 
• 196599-76-5 1-(4-trimethylsilylethynylphenyl)-3,3-tetramethylenetriazene 
• 220064-08-4 (8R,9S,13S,14S,17R)-3-Benzyloxy-13-methyl-17-[4-(pyrrolidin-1-ylazo)-phenyl]-7,8,9,11,12,13,14,15,16,17-decahydro-6H-cyclopenta[a]phenanthren-17-ol 
• 3406-76-6 (4-bromophenylthio)acetic acid 
• 589-87-7 1,4-bromoiodobenzene 

Relevant articles and documents

Sulfide synthesis through copper-catalyzed C-S bond formation under biomolecule-compatible conditions

We report here an efficient and mild method for constructing C-S bonds. The reactions were carried out with Na2S2O3 as a sulfurating reagent, CuSO4 as a catalyst, and water as solvent without any surfactant. The products were achieved in moderate to excellent yields at room temperature under air. Notably, this reaction is compatible with various biomolecules including amino acids, oligosaccharides, nucleosides, proteins, and cell lysates. This journal is

Suzuki-Miyaura cross-coupling reaction of 1-aryltriazenes with arylboronic acids catalyzed by a recyclable polymer-supported N-heterocyclic carbene-palladium complex catalyst

The Suzuki-Miyaura cross-coupling reaction of 1-aryltriazenes with arylboronic acids catalyzed by a recyclable polymer-supported Pd-NHC complex catalyst has been realized for the first time. The polymer-supported catalyst can be re-used several times still retaining high activity for this transformation. Various aryltriazenes were investigated as electrophilic substrates at room temperature to give biaryls in good to excellent yields and showed good chemoselectivity over aryl halides in the reactions.

New synthesis of phenylthioglycolic acids via related triazene compounds

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