5-Methyl-2-propan-2-ylcyclohexan-1-amine;hydrochloride

Base Information

Chemical Name:5-Methyl-2-propan-2-ylcyclohexan-1-amine;hydrochloride
CAS No.:75410-33-2
Molecular Formula:C10H21N
Molecular Weight:191.744
Hs Code.:
NSC Number:243754
DSSTox Substance ID:DTXSID10996849

Synonyms:75410-33-2;5-methyl-2-propan-2-ylcyclohexan-1-amine;hydrochloride;2-isopropyl-5-methylcyclohexylamine hydrochloride;menthylamine hydrochloride;SCHEMBL2123251;DTXSID10996849;NSC243754;NSC-243754;5-Methyl-2-(propan-2-yl)cyclohexan-1-amine--hydrogen chloride (1/1)

Suppliers and Price of 5-Methyl-2-propan-2-ylcyclohexan-1-amine;hydrochloride

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 5 raw suppliers

Chemical Property of 5-Methyl-2-propan-2-ylcyclohexan-1-amine;hydrochloride

Chemical Property:

Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:191.1440774
Heavy Atom Count:12
Complexity:120

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CCC(C(C1)N)C(C)C.Cl

Technology Process of 5-Methyl-2-propan-2-ylcyclohexan-1-amine;hydrochloride

There total 1 articles about 5-Methyl-2-propan-2-ylcyclohexan-1-amine;hydrochloride 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:

: 34048-57-2,75410-33-2,117947-19-0
(+/-)-neomenthylamine; hydrochloride

Guidance literature:: With hydrogenchloride;

Reference yield:

: 75410-33-2
(1R)-neoisomenthylamin; hydrochloride

: 920-46-7,26937-45-1
Methacryloyl chloride

: l-menthyl(meth)acrylamide

Guidance literature:: With triethylamine; In dichloromethane;

Reference yield:

: 112753-67-0
α,β-Difluoropropionyl chloride

: 34048-57-2,75410-33-2,117947-19-0
d-Menthylaminhydrochlorid

: 139680-35-6
d-Menthyl-α-fluoracrylamid

Guidance literature:: With triethylamine; Yield given. Multistep reaction; 1) CH₂Cl₂, 0 deg C, 30 min, 2) CH₂Cl₂, RT, overnight;
DOI:10.1016/S0022-1139(00)80116-5