Methyl 2-(1-naphthoylamino)benzoate

Base Information

Chemical Name:Methyl 2-(1-naphthoylamino)benzoate
CAS No.:75541-64-9
Molecular Formula:C₁₉H₁₅NO₃
Molecular Weight:305.333
Hs Code.:
DSSTox Substance ID:DTXSID501237259
ChEMBL ID:CHEMBL4745298

Synonyms:methyl 2-(1-naphthoylamino)benzoate;methyl 2-(naphthalene-1-carbonylamino)benzoate;CHEMBL4745298;DTXSID501237259;AKOS003052157;Methyl 2-[(1-naphthalenylcarbonyl)amino]benzoate;AN-652/11990804;75541-64-9

Suppliers and Price of Methyl 2-(1-naphthoylamino)benzoate

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
METHYL 2-(1-NAPHTHOYLAMINO)BENZOATE 95.00%
5MG
$ 495.36

Total 0 raw suppliers

Chemical Property of Methyl 2-(1-naphthoylamino)benzoate

Chemical Property:

XLogP3:4.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:305.10519334
Heavy Atom Count:23
Complexity:436

Purity/Quality:: METHYL 2-(1-NAPHTHOYLAMINO)BENZOATE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC(=O)C1=CC=CC=C1NC(=O)C2=CC=CC3=CC=CC=C32

Technology Process of Methyl 2-(1-naphthoylamino)benzoate

There total 4 articles about Methyl 2-(1-naphthoylamino)benzoate 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: 71.0%

: 86-55-5
1-naphthalenecarboxylic acid

: 134-20-3
2-carbomethoxyaniline

: 75541-64-9
methyl 2-(naphthalene-1-amido)benzoate

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1021/acsmedchemlett.0c00373

Reference yield:

: 134-20-3
2-carbomethoxyaniline

: 879-18-5
naphthalene-1-carbonic acid chloride

: 75541-64-9
methyl 2-(naphthalene-1-amido)benzoate

Guidance literature:: With triethylamine; In benzene; for 4h; Ambient temperature;
DOI:10.1080/00021369.1980.10864289

Reference yield:

: 86-55-5
1-naphthalenecarboxylic acid

: 75541-64-9
methyl 2-(naphthalene-1-amido)benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 1 h / 20 °C

2: triethylamine / dichloromethane / 2 h / 20 °C

With oxalyl dichloride; triethylamine; N,N-dimethyl-formamide; In dichloromethane;