Welcome to LookChem.com Sign In|Join Free
  • or
1,4,2,6-Dithiadiazine, 3,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89929-37-3

Post Buying Request

89929-37-3 Suppliers

Recommended suppliers

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

89929-37-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89929-37-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,2 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89929-37:
(7*8)+(6*9)+(5*9)+(4*2)+(3*9)+(2*3)+(1*7)=203
203 % 10 = 3
So 89929-37-3 is a valid CAS Registry Number.

89929-37-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-diphenyl-1,4,2,6-dithiadiazine

1.2 Other means of identification

Product number -
Other names 1,4,2,6-Dithiadiazine,3,5-diphenyl

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:89929-37-3 SDS

89929-37-3Relevant academic research and scientific papers

Preparation and reactions of 5-Aryl-1,4,2-dithiazolium salts

Yonemoto, Katsumi,Shibuya, Isao,Tsuchiya, Tohru,Masahiko Yasumoto,Taguchi, Yoichi

, p. 2933 - 2937 (2007/10/02)

S-Thioaroylsulfenamides (ArCSSNH2), formed by reaction of ArCSS-Na+ with hydroxylamine-O-sulfonic acid, were aroylated or acylated to give N-aroyl- or N-acyl-S-thioaroylsulfenamides, respectively, which were then cyclized with dehydration to afford 3-substituted 5-aryl-1,4,2-dithiazolium salts. The behavior of 3,5-diphenyl-1,4,2-dithiazolium Perchlorate toward nucleophiles such as active methylene and amino compounds was studied systematically. The reaction can be classified into two cases depending on fission modes of initial adducts, i.e., ring opening-ring closure reaction (Path B) and fragmentation of dithiazole ring (Path C), and in some cases the initial adducts were isolated.

Ring Expansion Reaction of Heterocyclic Cation Compounds by Incorporating One Nitrogen Atom Using I2-NH3 System

Yonemoto, Katsumi,Shibuya, Isao

, p. 89 - 90 (2007/10/02)

The reaction of various heterocyclic cation compounds with I2/NH4OH resulted in ring expansion on nitrogen atom.The similar ring expansion reaction occured on the corresponding triiodides with NH4OH.The reaction mechanism based on initial nucleophilic att

Organic Heterocyclothiazenes. Part 2. Reaction of Tetrasulphur Tetranitride with Phenylacetylene and Diphenylacetylene

Daley, Stephen T. A. K.,Rees, Charles W.

, p. 207 - 210 (2007/10/02)

The reaction of S4N4 with diphenylacetylene in boiling toluene has been found to give 3,4-diphenyl-1,2,5-thiadiazole (1) as the major product and 3,5-diphenyl-1,4,2,6-dithiadiazine (4), a new heterocyclic system, as a minor product.The same reaction with

Reactions of Tetrasulphur Tetranitride with Alkynes; 1,4,2,6-Dithiadiazines and 1,3,2-Dithiazoles

Daley, Stephen T. A. K.,Rees, Charles W.,Williams, David J.

, p. 57 - 59 (2007/10/02)

Reaction of S4N4 with diphenylacetylene and phenylacetylene gives two new, thermally stable heterocyclic systems, the 1,4,2,6-dithiadiazine (3) and the 1,3,2-dithiazolylimine (7), respectively, as minor products; these structures, determined by X-ray diff

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 89929-37-3