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1-Naphthalenecarboxylic acid, 2-[(phenylsulfonyl)amino]-

Base Information
  • Chemical Name:1-Naphthalenecarboxylic acid, 2-[(phenylsulfonyl)amino]-
  • CAS No.:677290-81-2
  • Molecular Formula:C17H13NO4S
  • Molecular Weight:327.361
  • Hs Code.:
  • ChEMBL ID:CHEMBL377198
  • DSSTox Substance ID:DTXSID20471157
1-Naphthalenecarboxylic acid, 2-[(phenylsulfonyl)amino]-

Synonyms:1-Naphthalenecarboxylic acid, 2-[(phenylsulfonyl)amino]-;677290-81-2;sulfonamide compound, 9;CHEMBL377198;SCHEMBL3986500;BDBM17603;DTXSID20471157;CXPIFTCBANXJNX-UHFFFAOYSA-N;PD083324;2-[(phenylsulfonyl)amino]-1-naphthoic acid;2-benzenesulfonamidonaphthalene-1-carboxylic acid

Suppliers and Price of 1-Naphthalenecarboxylic acid, 2-[(phenylsulfonyl)amino]-
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 1 raw suppliers
Chemical Property of 1-Naphthalenecarboxylic acid, 2-[(phenylsulfonyl)amino]-
Chemical Property:
  • XLogP3:3.8
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:4
  • Exact Mass:327.05652907
  • Heavy Atom Count:23
  • Complexity:521
Purity/Quality:

85.0-99.8% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)S(=O)(=O)NC2=C(C3=CC=CC=C3C=C2)C(=O)O
Technology Process of 1-Naphthalenecarboxylic acid, 2-[(phenylsulfonyl)amino]-

There total 43 articles about 1-Naphthalenecarboxylic acid, 2-[(phenylsulfonyl)amino]- 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:
Guidance literature:
2-aminonaphthalene-1-carboxylic acid; With pyridine; chloro-trimethyl-silane; In dichloromethane; at 20 ℃; for 4h;
benzenesulfonyl chloride; In ISOPROPYLAMIDE; at 20 ℃; for 16h;
Guidance literature:
With pyridine; chloro-trimethyl-silane; benzenesulfonyl chloride; trifluoroacetic acid; In dichloromethane; ISOPROPYLAMIDE; water; acetonitrile;
Guidance literature:
Multi-step reaction with 2 steps
1.1: aq. H2O2; NaOH
2.1: TMSCl / CH2Cl2
2.2: pyridine / CH2Cl2
With sodium hydroxide; chloro-trimethyl-silane; dihydrogen peroxide; In dichloromethane;
DOI:10.1016/j.bmcl.2006.03.085
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