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2,5-Dimethylpyridine-3-carboxaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1211522-52-9

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1211522-52-9 Usage

Chemical Family

2,5-Dimethylpyridine-3-carboxaldehyde belongs to the pyridine family.

Physical State

It is a yellow liquid.

Odor

It has a strong, unpleasant odor.

Usage

It is commonly used in the synthesis of pharmaceuticals, agrochemicals, dyes, and perfumes. It is also used as a flavoring agent in the food industry.

Medicinal Properties

It has been studied for its potential antifungal and antibacterial properties, making it a valuable compound in medicinal chemistry.

Toxicity

It is toxic and may cause irritation to the skin, eyes, and respiratory system if not handled properly.

Check Digit Verification of cas no

The CAS Registry Mumber 1211522-52-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,1,5,2 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1211522-52:
(9*1)+(8*2)+(7*1)+(6*1)+(5*5)+(4*2)+(3*2)+(2*5)+(1*2)=89
89 % 10 = 9
So 1211522-52-9 is a valid CAS Registry Number.

1211522-52-9SDS

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 2,5-dimethylpyridine-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2,5-Dimethylpyridine-3-carboxaldehyde

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:1211522-52-9 SDS

1211522-52-9Downstream Products

1211522-52-9Relevant academic research and scientific papers

Acetic Acid Promoted Redox Annulations with Dual C-H Functionalization

Zhu, Zhengbo,Seidel, Daniel

supporting information, p. 2841 - 2844 (2017/06/07)

Amines such as 1,2,3,4-tetrahydroisoquinoline undergo redox-neutral annulations with 2-alkylquinoline-3-carbaldehydes as well as the corresponding 4-alkyl isomers and pyridine analogues. These processes involve dual C-H bond functionalization. Acetic acid

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