N-isobutyrylbenzamide

Base Information Edit

Chemical Name:N-isobutyrylbenzamide
CAS No.:1738-54-1
Molecular Formula:C11H13NO2
Molecular Weight:191.23
Hs Code.:
DSSTox Substance ID:DTXSID30529471
Nikkaji Number:J2.395.950J
Wikidata:Q82399910
Mol file:1738-54-1.mol

Synonyms:N-isobutyrylbenzamide;1738-54-1;N-(2-Methylpropanoyl)benzamide;SCHEMBL12339108;DTXSID30529471;N-(2-methyl-propanoyl)-benzamide

Suppliers and Price of N-isobutyrylbenzamide

Supply Marketing:Edit

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 1 raw suppliers

Chemical Property of N-isobutyrylbenzamide Edit

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:191.094628657
Heavy Atom Count:14
Complexity:217

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C(=O)NC(=O)C1=CC=CC=C1

Technology Process of N-isobutyrylbenzamide

There total 17 articles about N-isobutyrylbenzamide 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%

: 4774-58-7
N-benzylisobutyramide

: 1738-54-1
N-isobutyrylbenzamide

Guidance literature:: With tert.-butylhydroperoxide; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; copper(I) bromide; In water; acetonitrile; at 20 ℃; for 8h;
DOI:10.1002/cjoc.201500190

Reference yield: 93.0%

: 60050-54-6
2-isopropyl-4-phenyl-4H-oxazol-5-one

: 1738-54-1
N-isobutyrylbenzamide

Guidance literature:: With triethylamine; In benzene; for 11h; Product distribution; Ambient temperature; various reagents, solvents and times;