2-(2-Methylphenyl)ethyl 3,5-dinitrobenzoate

Base Information

Chemical Name:2-(2-Methylphenyl)ethyl 3,5-dinitrobenzoate
CAS No.:22545-17-1
Molecular Formula:C₁₆H₁₄N₂O₆
Molecular Weight:330.297
Hs Code.:
NSC Number:115854
DSSTox Substance ID:DTXSID90297407
Wikidata:Q82038484
Mol file:22545-17-1.mol

Synonyms:22545-17-1;2-(2-methylphenyl)ethyl 3,5-dinitrobenzoate;NSC115854;DTXSID90297407;NSC-115854

Suppliers and Price of 2-(2-Methylphenyl)ethyl 3,5-dinitrobenzoate

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-(2-Methylphenyl)ethyl 3,5-dinitrobenzoate

Chemical Property:

Vapor Pressure:3.3E-10mmHg at 25°C
Boiling Point:502°Cat760mmHg
Flash Point:213.9°C
Density:1.35g/cm³
XLogP3:3.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:330.08518617
Heavy Atom Count:24
Complexity:450

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=CC=C1CCOC(=O)C2=CC(=CC(=C2)[N+](=O)[O-])[N+](=O)[O-]

Technology Process of 2-(2-Methylphenyl)ethyl 3,5-dinitrobenzoate

There total 2 articles about 2-(2-Methylphenyl)ethyl 3,5-dinitrobenzoate 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:

: 932-31-0
ortho-tolylmagnesium bromide

: 22545-17-1
3,5-dinitro-benzoic acid-(2-methyl-phenethyl ester)

Guidance literature:: Multi-step reaction with 2 steps

1: diethyl ether; benzene

With diethyl ether; benzene;
DOI:10.1021/jo01216a013