1-tert-Butylcyclohexane-1-carbonyl chloride

Base Information

Chemical Name:1-tert-Butylcyclohexane-1-carbonyl chloride
CAS No.:35618-41-8
Molecular Formula:C₁₁H₁₉ClO
Molecular Weight:202.724
Hs Code.:
DSSTox Substance ID:DTXSID30497343
Wikidata:Q82346787
Mol file:35618-41-8.mol

Synonyms:35618-41-8;1-tert-Butylcyclohexane-1-carbonyl chloride;SCHEMBL5730111;DTXSID30497343

Suppliers and Price of 1-tert-Butylcyclohexane-1-carbonyl chloride

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 1-tert-Butylcyclohexane-1-carbonyl chloride

Chemical Property:

Boiling Point:134-136 °C(Press: 20 Torr)
PSA：17.07000
Density:1.027±0.06 g/cm3(Predicted)
LogP:3.74840
XLogP3:4.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:202.1124429
Heavy Atom Count:13
Complexity:197

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)C1(CCCCC1)C(=O)Cl

Technology Process of 1-tert-Butylcyclohexane-1-carbonyl chloride

There total 1 articles about 1-tert-Butylcyclohexane-1-carbonyl chloride 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:

: 27334-43-6
1-tert-butyl-1-cyclohexyl-carboxylic acid

: 35618-41-8
1-tert-Butylcyclohexansaeurechlorid

Guidance literature:: With thionyl chloride;

Reference yield:

: 35618-41-8
1-tert-Butylcyclohexansaeurechlorid

: 41417-76-9
1-(1-t-Butylcyclohexan)-ethanol

Guidance literature:: Multi-step reaction with 2 steps

1: tetrahydrofuran

2: LiAlH₄ / dibutyl ether

With lithium aluminium tetrahydride; In tetrahydrofuran; dibutyl ether;