Welcome to LookChem.com Sign In|Join Free

CAS

  • or

76162-49-7

Post Buying Request

76162-49-7 Suppliers

Recommended suppliersmore

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

76162-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76162-49-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,1,6 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 76162-49:
(7*7)+(6*6)+(5*1)+(4*6)+(3*2)+(2*4)+(1*9)=137
137 % 10 = 7
So 76162-49-7 is a valid CAS Registry Number.

76162-49-7SDS

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 1,3,5-Triphenyl-2-pentene-1,5-dione

1.2 Other means of identification

Product number -
Other names 1,3,5-triphenyl-2-pentene-1,5-dione

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:76162-49-7 SDS

76162-49-7Relevant articles and documents

Regiocontrolled synthesis of 2,4,6-triarylpyridines from methyl ketones, electron-deficient acetylenes and ammonium acetate

Shabalin, Dmitrii A.,Dvorko, Marina Yu.,Schmidt, Elena Yu.,Trofimov, Boris A.

supporting information, p. 2703 - 2715 (2021/04/07)

A novel one-pot two-step approach for the synthesis of 2,4,6-triarylpyridinesvia t-BuOK/DMSO-promotedC-vinylation of a variety of methyl ketones with electron-deficient acetylenes (alkynones) followed by a cyclization of thein situgenerated unsaturated 1,5-dicarbonyl species with ammonium acetate has been developed. This approach possesses competitive advantages such as high regioselectivity, available starting materials and the absence of transition-metal catalysts, oxidants and undesirable byproducts. A wide synthetic utility of the developed approach was demonstrated by the synthesis of trisubstituted, tetrasubstituted and fused pyridines.

Free Radicals: XXVI. Reaction of 2,4,6-Triphenylpyranyl Radical with Oxygen

Tanaseichuk, B. S.,Pryanichnikova, M. K.,Tikhonova, L. G.

, p. 442 - 444 (2007/10/03)

Triphenylpyranyl radical reacts with oxygen to give 1,3,5-tiphenyl-2-pentene-1,5-dione, 3-phenoxymethyl-2,5-diphenylfuran, and 5-phenoxymethyl-2,4-diphenylfuran.

REACTION OF 2,4,6-TRIPHENYL-4H-PYRAN WITH THE VILSMEIER REAGENT

Koblik, A. V.,Suzdalev, K. F.

, p. 1206 - 1207 (2007/10/02)

-

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 76162-49-7