(1R,2R)-1,2,4-trimethylcyclopentane

Base Information

Chemical Name:(1R,2R)-1,2,4-trimethylcyclopentane
CAS No.:16883-48-0
Molecular Formula:C8H16
Molecular Weight:112.215
Hs Code.:2902199090
European Community (EC) Number:240-918-0
DSSTox Substance ID:DTXSID601025657
Nikkaji Number:J366.597F
Mol file:16883-48-0.mol

Synonyms:16883-48-0;Cis,trans,cis-1,2,4-trimethylcyclopentane;(1R,2R)-1,2,4-trimethylcyclopentane;Cyclopentane, 1,2,4-trimethyl-;(1alpha,2beta,4alpha)-1,2,4-Trimethylcyclopentane;Cyclopentane, 1,2,4-trimethyl-, (1.alpha.,2.beta.,4.alpha.)-;1,2,4-Trimethylcyclopentane #;PNUFYSGVPVMNRN-HTQZYQBOSA-N;DTXSID601025657;1beta,2alpha,4beta-Trimethylcyclopentane;Cis,trans,cis-1,2,4-trimethyl cyclopentane

Suppliers and Price of (1R,2R)-1,2,4-trimethylcyclopentane

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
1-trans-2-cis-4-Trimethylcyclopentane
100mg
$ 11825.00

Medical Isotopes, Inc.
1-trans-2-cis-4-Trimethylcyclopentane
50 mg
$ 9750.00

Total 4 raw suppliers

Chemical Property of (1R,2R)-1,2,4-trimethylcyclopentane

Chemical Property:

Vapor Pressure:21.8mmHg at 25°C
Melting Point:-130.78°C
Refractive Index:1.4081
Boiling Point:116.3°Cat760mmHg
Flash Point:9.2°C
PSA：0.00000
Density:0.754g/cm³
LogP:2.68850
XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:0
Exact Mass:112.125200510
Heavy Atom Count:8
Complexity:66.1

Purity/Quality:

99% ^*data from raw suppliers

1-trans-2-cis-4-Trimethylcyclopentane ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CC(C(C1)C)C
Isomeric SMILES:C[C@@H]1CC(C[C@H]1C)C

Technology Process of (1R,2R)-1,2,4-trimethylcyclopentane

There total 4 articles about (1R,2R)-1,2,4-trimethylcyclopentane 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: