(1-Bromoethyl)cyclohexane

Base Information

• Chemical Name: (1-Bromoethyl)cyclohexane
• CAS No.: 1073-42-3
• Molecular Formula: C8H15Br
• Molecular Weight: 191.111
• Hs Code.: 2903890090
• European Community (EC) Number: 824-444-7
• DSSTox Substance ID: DTXSID70513495
• Mol file: 1073-42-3.mol

Synonyms:(1-bromoethyl)cyclohexane;1073-42-3;1-bromoethylcyclohexane;Cyclohexane, (1-bromoethyl)-;(1-BROMOETHYL)-CYCLOHEXANE;SCHEMBL909432;DTXSID70513495;BAA07342;MFCD12065565;AKOS009988891;DS-3441;CS-0217325;EN300-736612;O10008

Chemical Property of (1-Bromoethyl)cyclohexane

Chemical Property:

• Boiling Point: 70.5-71 °C(Press: 6 Torr)
• PSA: 0.00000
• Density: 1.2096 g/cm3(Temp: 25 °C)
• LogP: 3.35010
• XLogP3: 3.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 1
• Exact Mass: 190.03571
• Heavy Atom Count: 9
• Complexity: 74.6

Purity/Quality:

97% ^*data from raw suppliers

(1-Bromoethyl)cyclohexane ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C1CCCCC1)Br

Technology Process of (1-Bromoethyl)cyclohexane

There total 2 articles about (1-Bromoethyl)cyclohexane 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:

→ 1-cyclohexylethyl bromide (1073-42-3)

Guidance literature:

With hydrogen bromide; benzene;

DOI:10.1021/ja01873a004

Reference yield:

→ 1-cyclohexylethyl bromide (1073-42-3)

Guidance literature:

(+-)-(1-Hydroxy-ethyl)-cyclohexan, PBr3, 0 - 10grad (1 /2h Dampfbad, dann ca. 12h Raumtemp.);

Reference yield: 58.0%

carbon dioxide (124-38-9,18923-20-1) + 1-cyclohexylethyl bromide (1073-42-3) → cyclohexanepropionic acid (701-97-3)

Guidance literature:

With nickel(II) iodide; manganese; 2,9-dihexyl-4,7-diphenyl-1,10-phenanthroline; In N,N-dimethyl-formamide; at 10 ℃; for 20h; under 760.051 Torr; regioselective reaction;

DOI:10.1038/nature22316

Downstream raw materials:

cyclohexanepropionic acid

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