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7-Methylquinoline-3-carbaldehyde, also known as 7-Methyl-3-formylquinoline, is a chemical compound that belongs to the class of quinoline derivatives. It is characterized by its distinctive aromatic structure and functional aldehyde group, making it a versatile intermediate in the synthesis of various pharmaceuticals and other organic molecules. Its unique structure and reactivity make it a valuable tool in the field of organic chemistry and drug development.

80231-38-5

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80231-38-5 Usage

Uses

Used in Pharmaceutical Research:
7-Methylquinoline-3-carbaldehyde is used as a building block in pharmaceutical research for the development of various compounds. Its distinctive aromatic structure and functional aldehyde group make it a versatile intermediate in the synthesis of pharmaceuticals.
Used in Organic Synthesis:
7-Methylquinoline-3-carbaldehyde is used as a key intermediate in organic synthesis, allowing for the creation of a wide range of organic molecules. Its unique reactivity and structure contribute to its utility in this field.
Used in Drug Development:
7-Methylquinoline-3-carbaldehyde is employed in drug development as a valuable tool for the synthesis of new and innovative pharmaceuticals. Its distinctive properties and reactivity make it an essential component in the development of novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 80231-38-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,3 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80231-38:
(7*8)+(6*0)+(5*2)+(4*3)+(3*1)+(2*3)+(1*8)=95
95 % 10 = 5
So 80231-38-5 is a valid CAS Registry Number.

80231-38-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-methylquinoline-3-carbaldehyde

1.2 Other means of identification

Product number -
Other names 7-METHYL-3-QUINOLINECARBOXALDEHYDE

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:80231-38-5 SDS

80231-38-5Downstream Products

80231-38-5Relevant academic research and scientific papers

An efficient synthesis of substituted quinolines

Tom,Ruel

, p. 1351 - 1355 (2007/10/03)

The addition of substituted anilines to "vinamidinium" bis-tetrafluoroborate salt 1 [2-dimethylaminomethylene-1,3-bis(dimethylimmonio)propane bis-tetrafluoroborate], followed by cyclization of the resulting imino-eneamine salt and hydrolysis of the masked aldehydes 2, provide the corresponding 3-formyl quinolines 3. While the condensation of both 1 and its analogous bis-perchlorate salt and amidines are known to provide pyrimidines, we believe this is the first example of a quinoline annulation sequence with "vinamidinium" bis-tetrafluoroborate salt 1 and anilines.

A Versatile New Synthesis of Quinolines and Related Fused Pyridines. Part 9. Synthetic Application of the 2-Chloroquinoline-3-carbaldehydes

Meth-Cohn, Otto,Narine, Bramha,Tarnowski, Brian,Hayes, Roy,Keyzad, Amitis,at al.

, p. 2509 - 2517 (2007/10/02)

The 2-chloro-groups of the title compounds have been replaced by H, I, OH, SR, Li, CO2H, CHO, Ph, piperidine, and N3 (giving a tetrazole).The aldehyde group has also been converted into oxime, hydrazone, and acrylic acid derivatives.From these and related

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