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

92180-70-6

Post Buying Request

92180-70-6 Suppliers

Recommended suppliers

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

92180-70-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92180-70-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,8 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 92180-70:
(7*9)+(6*2)+(5*1)+(4*8)+(3*0)+(2*7)+(1*0)=126
126 % 10 = 6
So 92180-70-6 is a valid CAS Registry Number.

92180-70-6SDS

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 3-methyl-1,5-diphenylpenta-2,4-dien-1-one

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:92180-70-6 SDS

92180-70-6Downstream Products

92180-70-6Relevant academic research and scientific papers

ACTION DES COMPOSES ORGANOMAGNESIENS SUR LES PYRONES-2 - VII ETUDE DE LA STABILITE RELATIVE DES HYDROXY-6 DYHIDRO-5,6 2H-PYRANNES ET DES CETOLS TAUTOMERES CORRESPONDANTS

Lhoste, P.,Moreau, M.,Dreux, J.

, p. 1551 - 1562 (2007/10/02)

In the reaction between organomagnesium compounds and 2-pyrones, the relative stability of the 6-hydroxy 5,6 2H-pyrans and their tautomeric forms (ketols) has no influence on the reaction pathway.When ethylenic ketols are obtained, the corresponding tautomeric dihydropyranols are prepared in a selective way by reaction of nucleophilic reagents on the 3,6-dihydropyrones.In the other hand, the exclusive formation either of the dihydropyranols or of the unsatured ketols E, during these two reactions, shows up that here is no equilibrium between these two entities in the experimental conditions.

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 92180-70-6