Welcome to LookChem.com Sign In|Join Free
  • or
1,2,5-Thiadiazolidine, 3-(2-naphthalenyl)-4-phenyl-, 1,1-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

194036-09-4

Post Buying Request

194036-09-4 Suppliers

Recommended suppliers

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

194036-09-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 194036-09-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,0,3 and 6 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 194036-09:
(8*1)+(7*9)+(6*4)+(5*0)+(4*3)+(3*6)+(2*0)+(1*9)=134
134 % 10 = 4
So 194036-09-4 is a valid CAS Registry Number.

194036-09-4SDS

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 3-(naphthalen-2-yl)-4-phenyl-1,2,5-thiadiazolidine 1,1-dioxide

1.2 Other means of identification

Product number -
Other names -

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:194036-09-4 SDS

194036-09-4Relevant academic research and scientific papers

Oxidation of 1,2,5-Thiadiazolidine 1,1-Dioxides: Synthesis of Diaryl 1,2-Diketones

Pansare, Sunil V.,Malusare, Mahesh G.

, p. 671 - 672 (2007/10/03)

Treatment of 3,4-diaryl 1,2,5-thiadiazolidine 1,1-dioxides with selenium dioxide followed by hydrolysis of the crude oxidation product furnishes the corresponding diaryl 1,2-diketones. Symmetrical and unsymmetrical diketones are readily prepared by this method.

Intramolecular imine cross-coupling in dibenzylidine sulfamides: Synthesis of unsymmetrical 1,2-diaryl ethanediamines

Pansare, Sunil V.,Malusare, Mahesh G.

, p. 2859 - 2862 (2007/10/03)

Intramolecular reductive cross-coupling of unsymmetrical dibenzylidene sulfamides generates the corresponding cyclic sulfamides in good yield. These intermediates are readily converted to the free, unsymmetrical 1,2-diaryl ethanediamines.

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 194036-09-4