Welcome to LookChem.com Sign In|Join Free

CAS

  • or

147878-14-6

Post Buying Request

147878-14-6 Suppliers

Recommended suppliersmore

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

147878-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 147878-14-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,8,7 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 147878-14:
(8*1)+(7*4)+(6*7)+(5*8)+(4*7)+(3*8)+(2*1)+(1*4)=176
176 % 10 = 6
So 147878-14-6 is a valid CAS Registry Number.

147878-14-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(5Z)-5-benzylidene-4-phenyl-1,3,4-selenadiazol-2-yl]ethanone

1.2 Other means of identification

Product number -
Other names 2-Benzylidene-3-phenyl-5-acetyl-1,3,4-selenadiazole

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:147878-14-6 SDS

147878-14-6Downstream Products

147878-14-6Relevant articles and documents

Reactions of thioamides and selenoamides with hydrazonoyl chlorides under phase-transfer conditions. A convenient method of preparation of Δ2-1,3,4-thiadiazolines and Δ2-1,3,4-selenadiazolines

Petrov,Abramov

, p. 331 - 343 (1998)

Reactions of enolizable thio- and selenoamides with hydrazonoyl chlorides in the presence of bases and phase-transfer catalysts result in 2-dialkylamino-Δ2-1,3,4-thia- and selenadiazolines. The reactions proceed through formation of correspondi

α,β-UNSATURATED THIOLATES AND THEIR ANALOGS IN CYCLOADDITION REACTIONS. XVIII. REACTION OF ENOLIZED DIALKYLSELENAMIDES WITH NITRILE IMINES IN THE PRESENCE OF BASES

Abramov, M. A.,Galishev, V. A.,Petrov, M. L.

, p. 1795 - 1804 (2007/10/02)

In reactions with nitrile imines in the presence of bases dialkylselenamides, which are capable of enolization, form derivatives of the five-membered heterocycles 1,3,4-selenadiazolines and not 1,3,4-selenadiazines as supposed earlier.It was established b

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 147878-14-6