10368-43-1

Basic information

• Product Name: (±)-trans-2-bromo-1,2-diphenylethan-1-ol
• Synonyms: (±)-trans-2-bromo-1,2-diphenylethan-1-ol
• CAS NO: 10368-43-1
• Molecular Weight: 277.161
• Mol File: 10368-43-1.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: (±)-trans-2-bromo-1,2-diphenylethan-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (±)-trans-2-bromo-1,2-diphenylethan-1-ol(10368-43-1)
• EPA Substance Registry System: (±)-trans-2-bromo-1,2-diphenylethan-1-ol(10368-43-1)

Safety Data

• Hazardous Substances Data: 10368-43-1(Hazardous Substances Data)

Upstream product

• 1439-07-2 trans-Stilbene oxide 
• 645-49-8 cis-stilben 
• 103-30-0 (E)-1,2-diphenyl-ethene 
• 1484-50-0 desyl bromide 
• 588-59-0 stilbene 
• 79-15-2 N-bromoacetamide 

Downstream Products

• 59982-09-1 erythro-1,2-diphenyl-1-bromo-2-fluoroethane 
• 59974-31-1 C₁₄H₁₂BrF 
• 947-91-1 Diphenylacetaldehyde 
• 103-30-0 (E)-1,2-diphenyl-ethene 
• 13440-24-9 anti-1,2-dibromo-1,2-diphenylethane 
• 13921-79-4 erythro-1-bromo-2-methoxy-1,2-diphenylethane 
• 13921-79-4 trans-(1-bromo-2-methoxyethane-1,2-diyl)dibenzene 
• 19456-17-8 (4R,5R)-4,5-diphenyl-1,3-dioxolan-2-one 
• 1439-07-2 trans-Stilbene oxide 
• 451-40-1 phenyl benzyl ketone 
• 66934-28-9 2-bromo-1,2-diphenylethyl benzoate 

Relevant articles and documents

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Regio-and stereoselective hydroxybromination and dibromination of olefins using ammonium bromide and oxone

An efficient protocol for the synthesis of vicinal bromohydrins and dibromides from olefins is presented. Various olefins are regio-and stereoselectively hydroxybrominated and dibrominated with anti fashion, following Markonikov's rule, using eco-friendly, non-toxic, and stable reagents such as NH4Br and oxone in CH3CN/H2O (1:1) and CH3CN without employing catalyst in moderate to excellent yields. Bromohydrins are formed instantaneously.

Organocatalysis in the stereoselective bromohydrin reaction of alkenes

An efficient regio- and stereo-selective (>99:1) trans-bromohydrination (bromohydroxylation and bromomethoxylation) of alkenes including α,β-unsaturated carbonyl compounds with N-bromosuccinimide (NBS) has been achieved by using 1.0 mol% of N,N'-diarylthi