Cyclohexanol, 2-bromo-

Base Information

• Chemical Name: Cyclohexanol, 2-bromo-
• CAS No.: 24796-87-0
• Molecular Formula: C6H11BrO
• Molecular Weight: 179.057
• Mol file: 24796-87-0.mol

Synonyms:trans-2-bromo-cyclohexanol;trans-1-bromo-2-hydroxycyclohexane;trans-2-bromocyclohexan-1-ol;2-bromocyclocyclohexanol;Cyclohexanol, 2-bromo-;(+/-)-(1S,2S)-2-bromocyclohexan-1-ol;(+/-)-trans-2-bromocyclohexan-1-ol;

Chemical Property of Cyclohexanol, 2-bromo-

Chemical Property:

• Refractive Index: 1.5169 (estimate)
• Boiling Point: 186.67°C (rough estimate)
• PSA: 20.23000
• Density: 1.4604
• LogP: 1.68480

Purity/Quality:

97% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of Cyclohexanol, 2-bromo-

There total 50 articles about Cyclohexanol, 2-bromo- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

cyclohexene (110-83-8) → 2-bromocyclocyclohexanol (2425-33-4,16536-57-5,24796-87-0,53023-24-8,53023-25-9,60933-67-7,5537-67-7)

Guidance literature:

With N-Bromosuccinimide; In water; at 0 - 25 ℃;

DOI:10.1016/S0040-4039(00)96738-8

Reference yield: 98.0%

cyclohexane-1,2-epoxide (286-20-4) → 2-bromocyclocyclohexanol (2425-33-4,16536-57-5,24796-87-0,53023-24-8,53023-25-9,60933-67-7,5537-67-7)

Guidance literature:

With hydrogen bromide; In chloroform; for 0.25h; Ambient temperature;

DOI:10.1016/S0040-4020(01)92271-9

Reference yield: 98.0%

cyclohexane-1,2-epoxide (286-20-4) → 2-bromo-cyclohexanol (24796-87-0,5537-67-7)

Guidance literature:

With N-methylpyrrolidine-2-one hydrotribromide; In acetonitrile; at 20 ℃; regioselective reaction;

DOI:10.1080/00397911.2010.493259

upstream raw materials:

2-bromocyclohexyl formate

cyclohexane-1,2-epoxide

cyclohexene

N-bromoacetamide

Downstream raw materials:

1-Brom-2-(2-chlorcyclohexyloxy)-cyclohexan

2-(prop-2-en-1-yl)cyclohexan-1-ol

(1R,2R)-trans-2-(N-methyl)amino-1-cyclohexanol

trans-2-(methylamino)cyclohexanol