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3-(4-CHLORO-PHENOXYMETHYL)-4-METHOXY-BENZALDEHYDE is a chemical compound characterized by a benzaldehyde group attached to a benzene ring, which features a chlorine atom and a methoxy group. 3-(4-CHLORO-PHENOXYMETHYL)-4-METHOXY-BENZALDEHYDE is known for its unique structural features, reactivity, and biological activity, making it a valuable building block in the synthesis of various compounds for different applications.

329222-77-7

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329222-77-7 Usage

Uses

Used in Pharmaceutical Industry:
3-(4-CHLORO-PHENOXYMETHYL)-4-METHOXY-BENZALDEHYDE is used as a building block for the synthesis of drugs due to its potential in the development of new pharmaceutical compounds. Its unique structure and reactivity contribute to the creation of molecules with specific therapeutic properties.
Used in Agricultural Industry:
3-(4-CHLORO-PHENOXYMETHYL)-4-METHOXY-BENZALDEHYDE is used as a building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its potential in the development of new agrochemicals is attributed to its unique structural features and biological activity, which can be harnessed to create effective and targeted compounds for agricultural use.

Check Digit Verification of cas no

The CAS Registry Mumber 329222-77-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,2,2 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 329222-77:
(8*3)+(7*2)+(6*9)+(5*2)+(4*2)+(3*2)+(2*7)+(1*7)=137
137 % 10 = 7
So 329222-77-7 is a valid CAS Registry Number.

329222-77-7Downstream Products

329222-77-7Relevant academic research and scientific papers

Alkylation of NH-, OH-, and SH-acids in the presence of potassium carbonate: 1. Functionalization of chloromethyl group of alkoxy-substituted aromatic aldehydes

Khachatryan,Razinov,Kolotaev,Belus?,Matevosyan

, p. 395 - 404 (2015/10/29)

An easily scalable, economocal, and more safe method for the preparation of 3-chloromethyl-4-methoxybenzaldehyde was developed. The latter was subjected to reactions with NH-, OH-, and SH-acids in the presence of potassium carbonate to obtain new aromatic aldehydes in high yields.

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