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Benzoic acid,2-(1H-pyrrol-2-ylmethylene)hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10344-26-0

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10344-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10344-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,4 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10344-26:
(7*1)+(6*0)+(5*3)+(4*4)+(3*4)+(2*2)+(1*6)=60
60 % 10 = 0
So 10344-26-0 is a valid CAS Registry Number.

10344-26-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N'-[(Z)-pyrrol-2-ylidenemethyl]benzohydrazide

1.2 Other means of identification

Product number -
Other names pyrrole-2-carbaldehyde benzoylhydrazone

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:10344-26-0 SDS

10344-26-0Relevant academic research and scientific papers

Synthesis and structure of arene ruthenium(II) complexes: One-pot catalytic approach to synthesis of bioactive quinolines under mild conditions

Subramanian, Muthumari,Sundar, Saranya,Rengan, Ramesh

, (2018)

Efficient catalytic one-step synthesis of substituted quinoline derivatives using newly synthesized Ru(II) half-sandwich complexes of the type [Ru(η6-p-cymene)Cl(L)] (L = pyrrole-2-aldehydehydrazones) under mild conditions is described. The synthesized complexes exhibit excellent catalytic activity towards the coupling of 2-amino alcohol with functionalized ketones and secondary alcohols in the optimal conditions and afforded the corresponding quinoline derivatives. The synthetic pathway proceeds with high atom efficiency via a sequence of acceptorless dehydrogenation and condensation steps. The maximum isolated yield of the product obtained was up to 97% using 0.3?mol% of catalyst loading for 5?h. These findings significantly advance the scope of the synthesis of bioactive heterocyclic compounds from readily available starting materials.

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