3-chloro-N-(1-naphthyl)benzamide

Base Information

Chemical Name:3-chloro-N-(1-naphthyl)benzamide
CAS No.:96963-51-8
Molecular Formula:C₁₇H₁₂ClNO
Molecular Weight:281.741
Hs Code.:
European Community (EC) Number:668-232-0
Nikkaji Number:J1.885.120B
Mol file:96963-51-8.mol

Synonyms:3-chloro-N-(naphthalen-1-yl)benzamide;3-chloro-N-(1-naphthyl)benzamide;96963-51-8;3-chloro-N-naphthalen-1-ylbenzamide;STK205226;AKOS003235009;AE-848/32184029

Suppliers and Price of 3-chloro-N-(1-naphthyl)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

Sigma-Aldrich
3-CHLORO-N-(1-NAPHTHYL)BENZAMIDE Aldrich
1ea
$ 57.00

American Custom Chemicals Corporation
3-CHLORO-N-(1-NAPHTHYL)BENZAMIDE 95.00%
5MG
$ 498.47

Total 3 raw suppliers

Chemical Property of 3-chloro-N-(1-naphthyl)benzamide

Chemical Property:

XLogP3:3.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:281.0607417
Heavy Atom Count:20
Complexity:346

Purity/Quality:: 3-CHLORO-N-(1-NAPHTHYL)BENZAMIDE Aldrich ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=CC=C2NC(=O)C3=CC(=CC=C3)Cl

Technology Process of 3-chloro-N-(1-naphthyl)benzamide

There total 2 articles about 3-chloro-N-(1-naphthyl)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:

: 535-80-8
3-chlorobenzoate

: 96963-51-8
3-Chloro-N-naphthalen-1-yl-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂

2: Na₂CO₃ / diethyl ether

With thionyl chloride; sodium carbonate; In diethyl ether;
DOI:10.1039/b210106h