Welcome to LookChem.com Sign In|Join Free

CAS

  • or

15046-75-0

Post Buying Request

15046-75-0 Suppliers

Recommended suppliersmore

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

15046-75-0 Usage

Uses

Sodium 2-Toluenesulfonate can be used for bactericidal composition.

Check Digit Verification of cas no

The CAS Registry Mumber 15046-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,4 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15046-75:
(7*1)+(6*5)+(5*0)+(4*4)+(3*6)+(2*7)+(1*5)=90
90 % 10 = 0
So 15046-75-0 is a valid CAS Registry Number.

15046-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name sodium 2-toluenesulfonate

1.2 Other means of identification

Product number -
Other names sodium o-toluenesulfonate

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:15046-75-0 SDS

15046-75-0Relevant articles and documents

Method for producing purified epoxy compound

-

, (2008/06/13)

A 2,3-epoxypropyl derivative or a 2-methyl-2,3-epoxypropyl derivative of a compound having carboxyl groups or amido groups is produced as a purified product having an epoxide equivalent of 1.0 to 1.1 times the theoretical epoxide equivalent of the derivat

Tin for Organic Synthesis, 7. New Regioselective Syntheses of Diaryl Sulfones, Arenesulfonamides, and Arenesulfonic Acid Sodium Salts

Neumann, Wilhelm P.,Wicenec, Christian

, p. 763 - 768 (2007/10/02)

The reaction of (trialkylstannyl)arenes 1 with corresponding reagents containing a chlorosulfonyl group leads, by exclusive ipso substitution, to important diaryl sulfones 2a - i, N-alkylarenesulfonamides 8a - f, and sodium arenesulfonates 13a - c in high yields under mild conditions.The specific leaving ability of the stannyl group allows, moreover, the preparation of arylsulfonyl isomers which are not accessible under the influence of the conventional directing forces of substituents.With N,N-dialkylamidosulfonyl chloride / AlCl3 complexes no destannylation takes place, but the first intramolecular sulfonyltin complex 11 is formed.This result is used to discuss details of the mechanism involved. Key Words: Aromatic substitution, electrophilic / Sulfones, synthesis of / Sulfonamides, synthesis of / Sulfonic acids, sodium salts, synthesis of/ Stannanes, trialkylaryl-, application of

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

What can I do for you?
Get Best Price

Get Best Price for 15046-75-0