Sorbanilide

Base Information Edit

Chemical Name:Sorbanilide
CAS No.:1483-88-1
Molecular Formula:C12H13NO
Molecular Weight:187.241
Hs Code.:
UNII:ZJJ70MU20Q
Nikkaji Number:J3.071.945J,J2.420.607F
Wikidata:Q27295622
ChEMBL ID:CHEMBL250216
Mol file:1483-88-1.mol

Synonyms:N-Phenylsorbamide;Sorbanilide;ZJJ70MU20Q;UNII-ZJJ70MU20Q;2,4-Hexadienamide, N-phenyl-, (2E,4E)-;1483-88-1;(2E,4E)-N-Phenyl-2,4-hexadienamide;2,4-Hexadienoanilide;(2E,4E)-N-phenylhexa-2,4-dienamide;N-Phenyl-2,4-hexadieneamide;CHEMBL250216;CTUGPZWRPKLTPL-XPQLPGEHSA-N;STK296263;AKOS003372885;(2E,4E)-N-Phenyl-2,4-hexadienamide #;(2E,4E)-N-phenyl-hexa-2,4-dienoic acid amide;Q27295622

Suppliers and Price of Sorbanilide

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 Sorbanilide Edit

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:187.099714038
Heavy Atom Count:14
Complexity:225

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC=CC=CC(=O)NC1=CC=CC=C1
Isomeric SMILES:C/C=C/C=C/C(=O)NC1=CC=CC=C1

Technology Process of Sorbanilide

There total 7 articles about Sorbanilide 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: 84.0%

: 143372-04-7
Hex-2-ynoic acid phenylamide

: 1483-88-1
N-phenylsorbamide

Guidance literature:: With acetic acid; triphenylphosphine; In xylene; at 140 ℃; for 14h;
DOI:10.1021/ja00046a062

Reference yield:

: 62-53-3
aniline

: 2614-88-2
sorbinyl chloride

: 1483-88-1
N-phenylsorbamide

Guidance literature:

Reference yield:

: 110-44-1,91751-55-2
sorbic Acid

: 1483-88-1
N-phenylsorbamide

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / 0.5 h / Heating

2: diethyl ether / 0.5 h / 20 °C

With thionyl chloride; In diethyl ether;