(1-Nitro-allyl)-benzene

Base Information

Chemical Name:(1-Nitro-allyl)-benzene
CAS No.:25236-39-9
Molecular Formula:C9H9 N O2
Molecular Weight:163.176
Hs Code.:
NSC Number:141638
DSSTox Substance ID:DTXSID40419273
Wikidata:Q82230222
Mol file:25236-39-9.mol

Synonyms:NSC141638;25236-39-9;(1-Nitro-allyl)-benzene;SCHEMBL7516376;SCHEMBL11897253;DTXSID40419273;NSC-141638;J-500250

Suppliers and Price of (1-Nitro-allyl)-benzene

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 (1-Nitro-allyl)-benzene

Chemical Property:

Vapor Pressure:0.00956mmHg at 25°C
Boiling Point:273.5°C at 760 mmHg
Flash Point:123.8°C
Density:1.113g/cm³
XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:163.063328530
Heavy Atom Count:12
Complexity:187

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC=C(C1=CC=CC=C1)[N+](=O)[O-]
Isomeric SMILES:C/C=C(\C1=CC=CC=C1)/[N+](=O)[O-]

Technology Process of (1-Nitro-allyl)-benzene

There total 3 articles about (1-Nitro-allyl)-benzene 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:

: 62634-59-7
1-nitro-1-phenyl-2-propanol

: 25236-39-9
2-phenyl-1-nitroprop-1-ene

Guidance literature:: With methanesulfonyl chloride; triethylamine; In dichloromethane; at 0 ℃; for 0.75h;
DOI:10.1016/S0040-4020(01)90296-0

Reference yield:

: 622-42-4
1-nitro-1-phenylmethane

: 25236-39-9
2-phenyl-1-nitroprop-1-ene

Guidance literature:: Multi-step reaction with 2 steps

1: basic aluminium oxide / 1.) 0 deg C, 5 h, 2.) room temperature, 20 h

2: methanesulfonyl chloride, triethylamine / CH₂Cl₂ / 0.75 h / 0 °C

With aluminum oxide; methanesulfonyl chloride; triethylamine; In dichloromethane;
DOI:10.1016/S0040-4020(01)90296-0