Welcome to LookChem.com Sign In|Join Free
  • or
Thiirane, triphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13896-15-6

Post Buying Request

13896-15-6 Suppliers

Recommended suppliers

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

13896-15-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13896-15-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,9 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13896-15:
(7*1)+(6*3)+(5*8)+(4*9)+(3*6)+(2*1)+(1*5)=126
126 % 10 = 6
So 13896-15-6 is a valid CAS Registry Number.

13896-15-6SDS

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 2,2,3-triphenylthiirane

1.2 Other means of identification

Product number -
Other names triphenylthiirane

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:13896-15-6 SDS

13896-15-6Relevant academic research and scientific papers

Structure and properties of a sulfur(IV)-sulfur(II)-bond compound: Reversible conversion of a sulfur-substituted organosulfurane into a thiol

Kano, Naokazu,Itoh, Yusuke,Watanabe, Yuki,Kusaka, Shinpei,Kawashima, Takayuki

supporting information; experimental part, p. 9430 - 9433 (2009/05/06)

(Figure Presented) A highly polar hypervalent SIV - S II bond was formed in the synthesis of a sulfur-substituted sulfurane (see scheme), which was crystallographically characterized. Reduction of the 1,2-dithietane gives the corresp

NEW THIOCARBONYL YLIDES FROM THIOBENZOPHENONE

Huisgen, Rolf,Xingya, Li

, p. 2363 - 2368 (2007/10/02)

Thiobenzophenone is converted to 1,3,4-thiadiazolines by reaction with diazoethane, phenyldiazomethane or diphenyldiazomethane at -78 deg C.Extrusion of nitrogen from the thiadiazolines furnishes thiocarbonyl ylides which, in turn, undergo electrocyclic r

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 13896-15-6