Cyclopentane, 1-methyl-1-nitro-

Base Information

Chemical Name:Cyclopentane, 1-methyl-1-nitro-
CAS No.:30168-50-4
Molecular Formula:C6H11 N O2
Molecular Weight:129.159
Hs Code.:
DSSTox Substance ID:DTXSID20184250
Nikkaji Number:J351.275D
Wikidata:Q83055149
Mol file:30168-50-4.mol

Synonyms:Cyclopentane, 1-methyl-1-nitro-;30168-50-4;1-methyl-1-nitrocyclopentane;SCHEMBL9452647;DTXSID20184250

Suppliers and Price of Cyclopentane, 1-methyl-1-nitro-

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 6 raw suppliers

Chemical Property of Cyclopentane, 1-methyl-1-nitro-

Chemical Property:

Vapor Pressure:0.813mmHg at 25°C
Boiling Point:182.4°Cat760mmHg
Flash Point:64.3°C
Density:1.05g/cm³
XLogP3:1.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:129.078978594
Heavy Atom Count:9
Complexity:122

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(CCCC1)[N+](=O)[O-]

Technology Process of Cyclopentane, 1-methyl-1-nitro-

There total 2 articles about Cyclopentane, 1-methyl-1-nitro- 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: 64.0%

: 133367-87-0
2-bromo-2-nitrohex-5-ene

: 109-49-9
5-Hexen-2-one

: 17397-24-9,17397-29-4,54774-27-5,626-94-8
hex-5-en-2-ol

: 30168-50-4
1-methyl-1-nitrocyclopentane

: 64999-95-7
2-nitrohex-5-ene

Guidance literature:: 2,2'-azobis(isobutyronitrile); In benzene; at 40 ℃; Product distribution; Mechanism; Irradiation; different concentrations of Bu₃SnH, without irradiation, absence of azobis(isobutyronitrile), presence of p-dinitrobenzene, presence of oxygen;