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3(2H)-Pyridazinone, 4,5-dihydro-5-(hydroxymethyl)-6-(4-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

95355-11-6

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95355-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95355-11-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,3,5 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 95355-11:
(7*9)+(6*5)+(5*3)+(4*5)+(3*5)+(2*1)+(1*1)=146
146 % 10 = 6
So 95355-11-6 is a valid CAS Registry Number.

95355-11-6SDS

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 4-(hydroxymethyl)-3-(4-methylphenyl)-4,5-dihydro-1H-pyridazin-6-one

1.2 Other means of identification

Product number -
Other names 4,5-dihydro-5-hydroxymethyl-6-p-tolylpyridazin-3(2H)-one

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:95355-11-6 SDS

95355-11-6Relevant academic research and scientific papers

Tetrahydropyridazinone derivatives, processes for their preparation and their use

-

, (2008/06/13)

Tetrahydropyridazinones of the formula I STR1 wherein R denotes an optionally substituted carbocyclic or heterocyclic radical, R1 denotes hydrogen; alkyl; aralkyl, which is optionally substituted in the aryl part; or acyl, and R2 den

Methylation of 5-Aldehydo-6-arylpyridazin-3(2H)-ones via Reaction with Dimethyl and Pentamethyl Cuprates

Shams, Nabil A.

, p. 536 - 542 (2007/10/02)

Me5Cu3Li2 in ether or ether-pentane mixtures, converts the title compounds efficiently into the corresponding 4-methyl derivatives (5) via conjugate methylation of either α,β-unsaturated aldehyde or N=C-C=C system, together with ca. 20percent of 1,2 adduc

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