Ameltolide

Base Information

Chemical Name:Ameltolide
CAS No.:787-93-9
Molecular Formula:C15H16 N2 O
Molecular Weight:240.305
Hs Code.:2924299090
European Community (EC) Number:804-885-1
UNII:F83240ZOVE
DSSTox Substance ID:DTXSID7052860
Nikkaji Number:J126.204A
Wikipedia:Ameltolide
Wikidata:Q4742349
NCI Thesaurus Code:C81472
Metabolomics Workbench ID:67628
ChEMBL ID:CHEMBL22916
Mol file:787-93-9.mol

Synonyms:4-amino-N-(2,6-dimethylphenyl)benzamide;ADD 75073;ameltolide;ameltolide monohydrobromide;ameltolide monohydrochloride;ameltolide sulfate;Lilly 201116;LY 201116;LY-201116

Suppliers and Price of Ameltolide

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

Matrix Scientific
4-Amino-N-(2,6-dimethylphenyl)benzamide
500mg
$ 199.00

Crysdot
4-Amino-N-(2,6-dimethylphenyl)benzamide 95+%
5g
$ 627.00

ChemBridge Corporation
4-amino-N-(2,6-dimethylphenyl)benzamide 95%
1 g
$ 140.00

American Custom Chemicals Corporation
4-AMINO-N-(2,6-DIMETHYLPHENYL)BENZAMIDE 95.00%
5MG
$ 496.39

AK Scientific
4-Amino-N-(2,6-dimethylphenyl)benzamide
500mg
$ 318.00

Total 6 raw suppliers

Chemical Property of Ameltolide

Chemical Property:

Vapor Pressure:8.41E-05mmHg at 25°C
Boiling Point:340.8°C at 760 mmHg
Flash Point:159.9°C
PSA：55.12000
Density:1.182g/cm³
LogP:3.79210
XLogP3:2.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:240.126263138
Heavy Atom Count:18
Complexity:274

Purity/Quality:

99%, ^*data from raw suppliers

4-Amino-N-(2,6-dimethylphenyl)benzamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C(=CC=C1)C)NC(=O)C2=CC=C(C=C2)N
Uses Anticonvulsant L.

Technology Process of Ameltolide

There total 13 articles about Ameltolide 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: 96.0%

: tert-butyl (4-((2,6-dimethylphenyl)carbamoyl)phenyl)carbamate

: 787-93-9
ameltolide

Guidance literature:: With hydrogenchloride; In water; at 23 ℃; for 2h; Inert atmosphere;
DOI:10.1021/acs.orglett.7b03214

Reference yield: 91.0%

: 64594-44-1
4-Nitro-N-(2,6-dimethylphenyl)benzamide

: 787-93-9
ameltolide

Guidance literature:: With cyclohexene; palladium on activated charcoal; In isopropyl alcohol; for 8h; Heating;
DOI:10.1021/jm9608772

Reference yield:

: 87-62-7
2,6-dimethylaniline

: 16106-38-0
4-aminobenzoyl chloride

: 787-93-9
ameltolide

Guidance literature:: 2,6-dimethylaniline; 4-aminobenzoyl chloride; In dichloromethane; at 20 ℃; for 1.5h;

With ethylenediamine; In ethanol; at 20 ℃; for 50h; Reflux;