N-(4-methyl-2-nitrophenyl)formamide

Base Information

Chemical Name:N-(4-methyl-2-nitrophenyl)formamide
CAS No.:71894-91-2
Molecular Formula:C₈H₈N₂O₃
Molecular Weight:180.163
Hs Code.:
European Community (EC) Number:652-052-4
Nikkaji Number:J3.521.341D

Synonyms:N-(4-methyl-2-nitrophenyl)formamide;2'-NITRO-PARA-FORMOTOLUIDIDE;SCHEMBL6182170;N-formyl-4-methyl-2-nitroaniline;QLNJWWYNJCJWFQ-UHFFFAOYSA-N;N-(4-methyl -2nitrophenyl)formamide;AKOS014313149;J3.521.341D

Suppliers and Price of N-(4-methyl-2-nitrophenyl)formamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of N-(4-methyl-2-nitrophenyl)formamide

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:180.05349212
Heavy Atom Count:13
Complexity:202

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC(=C(C=C1)NC=O)[N+](=O)[O-]

Technology Process of N-(4-methyl-2-nitrophenyl)formamide

There total 3 articles about N-(4-methyl-2-nitrophenyl)formamide 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: 90.0%

: 64-18-6
formic acid

: 89-62-3
4-methyl-2-nitroaniline

: 71894-91-2
N-(4-methyl-2-nitrophenyl)formamide

Guidance literature:: formic acid; 4-methyl-2-nitroaniline; In water; at 15 - 50 ℃; for 8h;

at 15 - 20 ℃;

Reference yield: 83.0%

: 57910-98-2
2-isocyanato-4-methyl-1-nitrobenzene

: 71894-91-2
N-(4-methyl-2-nitrophenyl)formamide

Guidance literature:: With zirconocene dichloride; lithium tri-t-butoxyaluminum hydride; In tetrahydrofuran; 2-methyltetrahydrofuran; at 0 - 20 ℃; for 1h; chemoselective reaction; Inert atmosphere;
DOI:10.1021/acs.orglett.6b01226