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(2-Iodoethenylidene)cyclohexane

Base Information Edit
  • Chemical Name:(2-Iodoethenylidene)cyclohexane
  • CAS No.:31814-67-2
  • Molecular Formula:C8H11I
  • Molecular Weight:234.08
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20497352
  • Nikkaji Number:J2.196.384D
  • Mol file:31814-67-2.mol
(2-Iodoethenylidene)cyclohexane

Synonyms:(2-Iodoethenylidene)cyclohexane;31814-67-2;DTXSID20497352

Suppliers and Price of (2-Iodoethenylidene)cyclohexane
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (2-Iodoethenylidene)cyclohexane Edit
Chemical Property:
  • XLogP3:2.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:0
  • Exact Mass:233.99055
  • Heavy Atom Count:9
  • Complexity:133
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CCC(=C=CI)CC1
Technology Process of (2-Iodoethenylidene)cyclohexane

There total 3 articles about (2-Iodoethenylidene)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:
Guidance literature:
Multi-step reaction with 2 steps
1: 86 percent / Cuprous bromide, ammonium bromide, copper powder / HBr / 1.5 h / 0 °C
2: 1.) n-butyllithium; 2.) 1,2-diiodoethane / 1.) Ether, hexane, -78 deg C, 30 min; 2.) 0 deg C, 1 h; Room temperature, 10 minute
With n-butyllithium; ammonium bromide; 1,2-Diiodoethane; copper; copper(I) bromide; In hydrogen bromide;
DOI:10.1021/jo01308a013
Guidance literature:
Multistep reaction; (i) Me2CuLi, Et2O, (ii) I2, 1,2-dimethoxy-ethane;
DOI:10.1039/c39770000761
Guidance literature:
With n-butyllithium; 1,2-Diiodoethane; Yield given. Multistep reaction; 1.) Ether, hexane, -78 deg C, 30 min; 2.) 0 deg C, 1 h; Room temperature, 10 minute;
DOI:10.1021/jo01308a013
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