(1R,2R)-trans-1-(ChloroMethyl)-2-Methylcyclopropane

Base Information

Chemical Name:(1R,2R)-trans-1-(ChloroMethyl)-2-Methylcyclopropane
CAS No.:10524-03-5
Molecular Formula:C₅H₉Cl
Molecular Weight:104.579
Hs Code.:
Mol file:10524-03-5.mol

Synonyms:

Suppliers and Price of (1R,2R)-trans-1-(ChloroMethyl)-2-Methylcyclopropane

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

TRC
(1R,2R)-trans-1-(Chloromethyl)-2-methylcyclopropane
250mg
$ 1540.00

Total 5 raw suppliers

Chemical Property of (1R,2R)-trans-1-(ChloroMethyl)-2-Methylcyclopropane

Chemical Property:

Purity/Quality:

98%,99%, ^*data from raw suppliers

(1R,2R)-trans-1-(Chloromethyl)-2-methylcyclopropane ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses (1R,2R)-trans-1-(Chloromethyl)-2-methylcyclopropane, can be used for the preparation of Mono- and bi-cyclic radicals containing the cyclopropylmethyl group, that can be used as a mechanistic probe and kinetic standards.

Technology Process of (1R,2R)-trans-1-(ChloroMethyl)-2-Methylcyclopropane

There total 3 articles about (1R,2R)-trans-1-(ChloroMethyl)-2-Methylcyclopropane 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:

: 6077-72-1
2-methylcyclopropanemethanol

: chloro(2-methylcyclopropyl)methane

: 10524-03-5,10524-04-6,89364-64-7
chloro(2-methylcyclopropyl)methane

Guidance literature:: With 1,1,1,3,3,3-hexachloro-propan-2-one; triphenylphosphine; at 0 - 20 ℃; for 3.25h; Title compound not separated from byproducts;
DOI:10.1021/jo047822p