Acetamide, N-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)- (9CI)

Base Information

Chemical Name:Acetamide, N-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)- (9CI)
CAS No.:102616-87-5
Molecular Formula:C₉H₉N₃O₂
Molecular Weight:191.189
Hs Code.:
Mol file:102616-87-5.mol

Synonyms:Acetamide, N-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)- (9CI)

Suppliers and Price of Acetamide, N-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)- (9CI)

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

AccelPharmtech
N-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-Acetamide 97.00%
5G
$ 2960.00

Total 1 raw suppliers

Chemical Property of Acetamide, N-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)- (9CI)

Chemical Property:

PSA：66.89000
LogP:0.49260

Purity/Quality:: N-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)-Acetamide 97.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Acetamide, N-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)- (9CI)

There total 2 articles about Acetamide, N-(2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)- (9CI) 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: 41.0%

: 541-41-3
chloroformic acid ethyl ester

: 6299-91-8
N'-(2-aminophenyl)acetohydrazide

: 102616-87-5
1-acetamido-2-benzimidazolinone

Guidance literature:: In pyridine; 1) room temp., overnight; 2) reflux, 23 h;
DOI:10.1002/jhet.5570220433

Reference yield:

: 14674-17-0
acetic acid 2-(2-nitrophenyl)hydrazide

: 102616-87-5
1-acetamido-2-benzimidazolinone

Guidance literature:: Multi-step reaction with 2 steps

1: 4.82 g / H₂ / 5percent Pd/C / methanol

2: 41 percent / pyridine / 1) room temp., overnight; 2) reflux, 23 h

With hydrogen; palladium on activated charcoal; In pyridine; methanol;
DOI:10.1002/jhet.5570220433

Reference yield: 42.0%

: 102616-87-5
1-acetamido-2-benzimidazolinone

: 102616-88-6
1-ethylamino-2-benzimidazolinone

Guidance literature:: With sodium bis(2-methoxyethoxy)aluminium dihydride; In tetrahydrofuran; toluene; 1) room temp., overnight; 2) relux, 3.25 h;
DOI:10.1002/jhet.5570220433