Glisolamide

Base Information

Chemical Name:Glisolamide
CAS No.:24477-37-0
Molecular Formula:C₂₀H₂₆N₄O₅S
Molecular Weight:434.516
Hs Code.:
UNII:F83U6T74XR
DSSTox Substance ID:DTXSID00179245
Nikkaji Number:J16.701K
Wikidata:Q27277793
NCI Thesaurus Code:C72800
ChEMBL ID:CHEMBL2106775
Mol file:24477-37-0.mol

Synonyms:glisolamide;glysolamide;N-(4-(beta-(5-methylisoxazol-3-carboxamido)-ethyl)benzenesulfonyl)-N(1)-cyclohexylurea

Suppliers and Price of Glisolamide

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

Total 6 raw suppliers

Chemical Property of Glisolamide

Chemical Property:

Melting Point:198°C
Refractive Index:1.6000 (estimate)
Boiling Point:°Cat760mmHg
PKA:5.09±0.10(Predicted)
Flash Point:°C
PSA：138.78000
Density:1.35g/cm³
LogP:4.52960
XLogP3:3.3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:7
Exact Mass:434.16239112
Heavy Atom Count:30
Complexity:682

Purity/Quality:: 98%Min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC(=NO1)C(=O)NCCC2=CC=C(C=C2)S(=O)(=O)NC(=O)NC3CCCCC3

Technology Process of Glisolamide

There total 4 articles about Glisolamide 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:

: 39499-34-8
5-methyl-3-isoxazolyl chloride

: 24477-37-0
5-methyl-isoxazole-3-carboxylic acid 4-(cyclohexylcarbamoyl-sulfamoyl)-phenethylamide

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine

2: K₂CO₃ / butan-2-one

With potassium carbonate; In pyridine; butanone;

Reference yield:

: 6325-22-0,42286-14-6
chlorhydrate de (β-aminoethyl)-4 benzenesulfonamide

: 24477-37-0
5-methyl-isoxazole-3-carboxylic acid 4-(cyclohexylcarbamoyl-sulfamoyl)-phenethylamide

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine

2: K₂CO₃ / butan-2-one

With potassium carbonate; In pyridine; butanone;