Benzamide, 2-nitro-N-2-propenyl-

Base Information

Chemical Name:Benzamide, 2-nitro-N-2-propenyl-
CAS No.:88229-25-8
Molecular Formula:C10H10N2O3
Molecular Weight:206.201
Hs Code.:
DSSTox Substance ID:DTXSID70394443
Wikidata:Q82193828

Synonyms:Benzamide, 2-nitro-N-2-propenyl-;88229-25-8;Oprea1_838986;SCHEMBL7084989;DTXSID70394443;AKOS002944946

Suppliers and Price of Benzamide, 2-nitro-N-2-propenyl-

Supply Marketing:

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

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Chemical Property of Benzamide, 2-nitro-N-2-propenyl-

Chemical Property:

XLogP3:0.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:206.06914219
Heavy Atom Count:15
Complexity:260

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Benzamide, 2-nitro-N-2-propenyl-

There total 3 articles about Benzamide, 2-nitro-N-2-propenyl- 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: 95.0%

: 107-11-9,30551-89-4
1-amino-2-propene

: 610-14-0
2-nitrobenzyl chloride

: 88229-25-8
N-allyl-2-nitrobenzamide

Guidance literature:: In benzene; for 18h;
DOI:10.1021/je00036a040

Reference yield:

: 4943-82-2
N-allyl-2-aminobenzamide

: 88229-25-8
N-allyl-2-nitrobenzamide

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In methanol; water; at 27 ℃; for 8h;
DOI:10.1039/c5ra23013f

Reference yield:

: 118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4
anthranilic acid

: 88229-25-8
N-allyl-2-nitrobenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 12 h / 0 - 20 °C

2: 3-chloro-benzenecarboperoxoic acid / water; methanol / 8 h / 27 °C

With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 3-chloro-benzenecarboperoxoic acid; In methanol; dichloromethane; water;
DOI:10.1039/c5ra23013f