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132814-17-6

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132814-17-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132814-17-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,8,1 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 132814-17:
(8*1)+(7*3)+(6*2)+(5*8)+(4*1)+(3*4)+(2*1)+(1*7)=106
106 % 10 = 6
So 132814-17-6 is a valid CAS Registry Number.

132814-17-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-phenyl-5-hydroxymethyl-4,5-dihydro-2H-pyridazin-3-one acetate

1.2 Other means of identification

Product number -
Other names 6-phenyl-5-hydroxymethyl-4,5-dihydro-3(2H)-pyridazinine acetate

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:132814-17-6 SDS

132814-17-6Relevant articles and documents

Pyridazine derivatives. XIX: Functionalization studies at the 5 position in the 6-phenyl-3(2H)-pyridazinone system

Sotelo, Eddy,Ravina, Enrique,Estevez, Isabel

, p. 985 - 990 (2007/10/03)

A series of 6-phenyl-3(2H)-pyridazinones bearing different substitution at the 5 position of the pyridazinone ring were prepared in the search for new platelet aggregation inhibitors. The structure of the final compounds was determined on the basis of spectroscopics methods.

PYRIDAZINE DERIVATIVES, IX. SYNTHESIS OF 2H-PYRIDAZIN-3-ONES WITH AROYLPIPERAZINYL GROUPS

Ravina, Enrique,Teran, Carmen,Santana, Lourdes,Garcia, Neftali,Estevez, Isabel

, p. 1967 - 1974 (2007/10/02)

Several 2H-pyridazin-3-ones with phenyl- or 2-furoylpiperazinyl group, have been prepared. 6-Phenyl-5-(N4-aroyl-N1-piperazinyl)-2H-pyridazin-3-ones were obtained by nucleophilic substitution of the chlorine atom of 6-phenyl-5-chloro-

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