2-Chloro-1-(3-nitrophenyl)ethanol

Base Information

Chemical Name:2-Chloro-1-(3-nitrophenyl)ethanol
CAS No.:13425-36-0
Molecular Formula:C8H8 Cl N O3
Molecular Weight:201.609
Hs Code.:
DSSTox Substance ID:DTXSID10436775
Nikkaji Number:J2.995.134I
Mol file:13425-36-0.mol

Synonyms:2-chloro-1-(3-nitrophenyl)ethanol;13425-36-0;Benzenemethanol, alpha-(chloromethyl)-3-nitro- (9CI);2-Chloro-1-(3-nitrophenyl)ethan-1-ol;SCHEMBL6742897;DTXSID10436775;1-(m-Nitrophenyl)-2-chloroethanol;AKOS017559739;EN300-1968163

Suppliers and Price of 2-Chloro-1-(3-nitrophenyl)ethanol

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 2-Chloro-1-(3-nitrophenyl)ethanol

Chemical Property:

PSA：66.05000
LogP:2.39020
XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:201.0192708
Heavy Atom Count:13
Complexity:183

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC(=C1)[N+](=O)[O-])C(CCl)O

Technology Process of 2-Chloro-1-(3-nitrophenyl)ethanol

There total 6 articles about 2-Chloro-1-(3-nitrophenyl)ethanol 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: 84.0%

: 586-39-0,51209-60-0
1-nitro-3-vinyl-benzene

: 13425-36-0,329348-23-4
()-2-chloro-1-(3-nitrophenyl)ethanol

Guidance literature:: With 1,3-dichloro-5,5-dimethylhydantoin; (2S,3S)-3-hydroxy-2-(4-methylphenylsulfonamido)butanoic acid; water; In acetone; at 20 ℃; for 1h; regioselective reaction;
DOI:10.1016/j.tet.2011.06.077