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1196154-24-1

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1196154-24-1 Usage

Reactivity

Highly reactive aldehyde

Utility

Commonly used in organic synthesis and pharmaceutical research
Acts as a building block in the synthesis of complex organic molecules

Functional Group

Chloromethyl group at the 6th position of the pyridine ring
Aldehyde group

Applications

Valuable reagent in the formation of heterocyclic compounds
Important in the development of new drugs and agrochemicals

Modification of Reactivity

Presence of chlorine atom modifies reactivity

Versatility

Useful in various reactions

Importance

Crucial in organic chemistry and pharmaceutical research

Check Digit Verification of cas no

The CAS Registry Mumber 1196154-24-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,6,1,5 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1196154-24:
(9*1)+(8*1)+(7*9)+(6*6)+(5*1)+(4*5)+(3*4)+(2*2)+(1*4)=161
161 % 10 = 1
So 1196154-24-1 is a valid CAS Registry Number.

1196154-24-1SDS

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 6-(chloromethyl)pyridine-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 6-chloromethyl-pyrid-3-yl-carbaldehyde

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:1196154-24-1 SDS

1196154-24-1Downstream Products

1196154-24-1Relevant articles and documents

Towards the synthesis of substituted porphyrins by a pyridyl group bearing a reactive functionality

Ojaimi, Maya El,Habermeyer, Benoit,Gros, Claude P.,Barbe, Jean-Michel

, p. 469 - 480 (2011/03/20)

Pyridyl-substituted porphyrins bearing a reactive functionality were prepared via Suzuki cross-coupling reactions and resulted in very good yields. These compounds are precursors of new porphyrin architectures able to coordinate two metals: one in the porphyrin core and the second around the pyridyl moiety. During the coupling reactions, a higher reactivity of a chloro picolyl group was evidenced compared to a bromo function on the same reacting molecule.

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