2-Amino-6-methyl-N-(o-tolyl)benzamide

Base Information

Chemical Name:2-Amino-6-methyl-N-(o-tolyl)benzamide
CAS No.:371244-06-3
Molecular Formula:C15H16N2O
Molecular Weight:240.305
Hs Code.:2924299090
DSSTox Substance ID:DTXSID90602759
Nikkaji Number:J2.446.924G
Wikidata:Q82499932
Mol file:371244-06-3.mol

Synonyms:371244-06-3;2-Amino-6-methyl-N-(o-tolyl)benzamide;2-amino-6-methyl-N-o-tolylbenzamide;2-amino-6-methyl-N-(2-methylphenyl)benzamide;SCHEMBL1296757;DTXSID90602759;DJCBUJASTUIFPG-UHFFFAOYSA-N;WPA24406;MFCD09806572;AKOS000163232;AM805679;AS-62332;DB-346870

Suppliers and Price of 2-Amino-6-methyl-N-(o-tolyl)benzamide

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

Crysdot
2-Amino-6-methyl-N-(o-tolyl)benzamide 95+%
5g
$ 617.00

American Custom Chemicals Corporation
2-AMINO-6-METHYL-N-O-TOLYLBENZAMIDE 95.00%
5MG
$ 503.91

Alichem
2-Amino-6-methyl-N-(o-tolyl)benzamide
25g
$ 746.46

Alichem
2-Amino-6-methyl-N-(o-tolyl)benzamide
5g
$ 604.31

Acrotein
2-Amino-6-methyl-N-(o-tolyl)benzamide 97%
1g
$ 94.40

Total 6 raw suppliers

Chemical Property of 2-Amino-6-methyl-N-(o-tolyl)benzamide

Chemical Property:

PSA：58.61000
LogP:4.10310
Storage Temp.:2-8°C(protect from light)
XLogP3:3.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:240.126263138
Heavy Atom Count:18
Complexity:292

Purity/Quality:

99% ^*data from raw suppliers

2-Amino-6-methyl-N-(o-tolyl)benzamide 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C(=CC=C1)N)C(=O)NC2=CC=CC=C2C

Technology Process of 2-Amino-6-methyl-N-(o-tolyl)benzamide

There total 3 articles about 2-Amino-6-methyl-N-(o-tolyl)benzamide 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: 91.0%

: 4389-50-8
2-amino-6-methylbenzoic acid

: 95-53-4
o-toluidine

: 371244-06-3
2-amino-6-methyl-N-o-tolylbenzamide

Guidance literature:: 2-amino-6-methylbenzoic acid; With thionyl chloride; In toluene; for 1h; Heating;

o-toluidine; In tetrahydrofuran; for 18h; Further stages.; Heating;
DOI:10.1021/ol070276c

Reference yield:

: 2-amino-6-methylbenzoyl chloride

: 95-53-4
o-toluidine

: 371244-06-3
2-amino-6-methyl-N-o-tolylbenzamide

Guidance literature:: In chloroform; for 3h; Heating / reflux;

Reference yield:

: 4389-50-8
2-amino-6-methylbenzoic acid

: 371244-06-3
2-amino-6-methyl-N-o-tolylbenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / toluene / 1 h / 110 °C

2: tetrahydrofuran / 2 h / 0 - 80 °C

With thionyl chloride; In tetrahydrofuran; toluene;