Welcome to LookChem.com Sign In|Join Free
  • or
N-[(4-chlorophenyl)carbamoyl]benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

102607-82-9

Post Buying Request

102607-82-9 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

102607-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 102607-82-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,6,0 and 7 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102607-82:
(8*1)+(7*0)+(6*2)+(5*6)+(4*0)+(3*7)+(2*8)+(1*2)=89
89 % 10 = 9
So 102607-82-9 is a valid CAS Registry Number.

102607-82-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(((4-chlorophenyl)amino)carbonyl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names N-([(4-chlorophenyl)amino]carbonyl)benzenesulfonamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:102607-82-9 SDS

102607-82-9Downstream Products

102607-82-9Relevant academic research and scientific papers

A general acid-catalyzed anion breakdown associated with an E1cB reaction in the hydrolysis of aryl N-(substituted phenylsulfonyl)carbamates

Vigroux, Alain,Bergon, Michel,Bergonzi, Catherine,Tisnès, Pierre

, p. 11787 - 11796 (2007/10/02)

The hydrolysis of aryl N-(substituted phenylsulfonyl)carbamates at 50 °C in the pH range 0-13.5 leading to substituted benzenesulfonamides and phenols involves acyl group transfer. Reaction rates were measured spectrophotometrically and are independent of

Novel agents effective against solid tumors: The diarylsulfonylureas. Synthesis, activities, and analysis of quantitative structure-activity relationships

Howbert,Grossman,Crowell,Rieder,Harper,Kramer,Tao,Aikins,Poore,Rinzel,Grindey,Shaw,Todd

, p. 2393 - 2407 (2007/10/02)

A series of diarylsulfonylureas with exceptionally broad-spectrum activity against syngeneic rodent solid tumors in vivo is described. Their discovery resulted from a program dedicated to in vivo screening for novel oncolytics in solid tumor models, rather than traditional ascites leukemia models. The structures, oral efficacy, side-effect profile, and mechanism of action of these sulfonylureas appear to be distinct from previously known classes of oncolytics. An extensive series of analogues was prepared to probe structure-activity relationships (SAR), with particular focus on the substituent patterns of each aryl domain. Quantitative analysis of these substituent SARs, using the method of cluster significance analysis, showed the lipophilicity of the substituents to be the dominant determinant of activity. One compound from the series, LY186641 (104, sulofenur), has progressed to Phase I clinical trials as an antitumor drug.

N([(4-trifluoromethylphenyl)amino]carbonyl)benzene sulfonamides

-

, (2008/06/13)

This invention provides the use of certain benzenesulfonamide derivatives in the treatment of susceptible neoplasms in mammals. Also provided are certain novel benzenesulfonamide derivatives and their pharmaceutical formulations.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 102607-82-9