Glypinamide

Base Information

Chemical Name:Glypinamide
CAS No.:1228-19-9
Molecular Formula:C13H18 Cl N3 O3 S
Molecular Weight:331.823
Hs Code.:2935009090
NSC Number:70737
UNII:ORE084U8IP
DSSTox Substance ID:DTXSID70153719
Nikkaji Number:J9.495A
Wikidata:Q27285802
NCI Thesaurus Code:C65811
ChEMBL ID:CHEMBL2106693
Mol file:1228-19-9.mol

Synonyms:Glypinamide;Azepinamide;Parinase;1228-19-9;Glypinamide [INN];NSC-70737;UNII-ORE084U8IP;ORE084U8IP;NSC70737;NSC 70737;N-(p-Chlorophenyl)sulfonyl N'-hexahydroazepinourea;1-((p-Chlorophenyl)sulfonyl)-3-(hexahydro-1H-azepin-1-yl)urea;Urea, 1-[(p-chlorophenyl)sulfonyl]-3-(hexahydro-1H-azepin-1-yl)-;Benzenesulfonamide, 4-chloro-N-[[(hexahydro-1H-azepin-1-yl)amino]carbonyl]-;1-(((((4-Chlorophenyl)sulfonyl)amino)carbonyl)amino)azepane;1-[({[(4-chlorophenyl)sulfonyl]amino}carbonyl)amino]azepane;1-(azepan-1-yl)-3-(4-chlorophenyl)sulfonylurea;GLYPINAMIDE [MI];NCIOpen2_008327;SCHEMBL343885;CHEMBL2106693;DTXSID70153719;CHEBI:135415;C13-H18-Cl-N3-O3-S;LS-159596;1-(azepan-1-yl)-3-(4-chlorophenyl)sulfonyl-urea;Q27285802;1-((p-Chlorophenyl)-sulfonyl)-3-(hexahydro-1H-azepin-1-yl)urea.;Urea, {1-[(p-chlorophenyl)sulfonyl]-3-(hexahydro-1H-azepin-1-yl)-};Benzenesulfonamide, {4-chloro-N-[[(hexahydro-1H-azepin-1-yl)amino]carbonyl]-}

Suppliers and Price of Glypinamide

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

American Custom Chemicals Corporation
1-[(([(4-CHLOROPHENYL)SULFONYL]AMINO)CARBONYL)AMINO]AZEPANE 95.00%
5MG
$ 501.50

Total 7 raw suppliers

Chemical Property of Glypinamide

Chemical Property:

Melting Point:197-198.5°
Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：86.89000
Density:1.4g/cm³
LogP:3.91940
XLogP3:1.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:331.0757403
Heavy Atom Count:21
Complexity:436

Purity/Quality:

99% ^*data from raw suppliers

1-[(([(4-CHLOROPHENYL)SULFONYL]AMINO)CARBONYL)AMINO]AZEPANE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCCN(CC1)NC(=O)NS(=O)(=O)C2=CC=C(C=C2)Cl

Technology Process of Glypinamide

There total 1 articles about Glypinamide 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:

: 1228-19-9
tolazamide

Guidance literature:: N-<4-Chlor-benzolsulfonyl>-carbamidsaeure-methylester, 1-Amino-hexamethylenimin (2 h, 130grad/1at; 2 h 130grad/25mm);

Reference yield:

: 1228-19-9
tolazamide

: 70-55-3
toluene-4-sulfonamide

: 52206-35-6
Azepan-1-ylamine; hydrochloride

Guidance literature:: With phosphate buffer; chloride ions; at 37 ℃; for 24h; Product distribution; various concentrations of anions and cations, with and without human serum proteins;
DOI:10.1248/cpb.34.2957