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2-(Benzyloxy)-5-formylbenzoic acid is a benzene compound that features a benzyl ether and a formyl group attached to the benzene ring. It belongs to the benzoic acid family and is widely recognized as a versatile building block in organic synthesis. This chemical is celebrated for its contributions to the production of pharmaceuticals and agrochemicals, and it serves as a starting material for synthesizing a range of bioactive compounds. Its unique properties and broad applications render it an indispensable compound in medicinal and organic chemistry.

169209-25-0

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169209-25-0 Usage

Uses

Used in Pharmaceutical Industry:
2-(Benzyloxy)-5-formylbenzoic acid is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be readily modified and incorporated into complex molecular structures. Its presence in drug molecules can enhance their therapeutic effects and pharmacological properties, making it a valuable component in the development of new medications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(Benzyloxy)-5-formylbenzoic acid is utilized as a starting material for the production of pesticides and other agrochemicals. Its chemical properties allow for the creation of compounds that can effectively control pests and diseases in agriculture, thereby contributing to increased crop yields and protection of plants.
Used in Organic Synthesis:
2-(Benzyloxy)-5-formylbenzoic acid is employed as a fundamental building block in organic synthesis for its reactivity and capacity to form a variety of derivatives. Its presence in synthetic pathways enables the creation of diverse chemical entities with potential applications in various fields, including materials science, fragrances, and dyes.
Used in the Synthesis of Bioactive Compounds:
As a starting material, 2-(Benzyloxy)-5-formylbenzoic acid is harnessed in the synthesis of bioactive compounds that possess specific biological activities. These compounds can be used in research and development for potential applications in medicine, such as drug discovery, or in other industries where bioactive substances are required.

Check Digit Verification of cas no

The CAS Registry Mumber 169209-25-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,2,0 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 169209-25:
(8*1)+(7*6)+(6*9)+(5*2)+(4*0)+(3*9)+(2*2)+(1*5)=150
150 % 10 = 0
So 169209-25-0 is a valid CAS Registry Number.

169209-25-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-formyl-2-phenylmethoxybenzoic acid

1.2 Other means of identification

Product number -
Other names -

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:169209-25-0 SDS

169209-25-0Relevant academic research and scientific papers

NOVEL COMPOUNDS

-

, (2011/04/25)

The present invention discloses novel compounds inhibiting LRRK2 kinase activity, the preparation processes thereof, the compositions containing them, as well as the use in treating diseases characterized by LRRK2 kinase activity, particularly Parkinson's disease and Alzheimer's disease.

Synthesis of aromatic carboxylic acids by carbonylation of aryl halides in the presence of epoxide-modified cobalt carbonyls as catalysts

Boyarskii,Zhesko,Lanina

, p. 1844 - 1848 (2007/10/03)

A new procedure was developed for synthesis of aromatic and heteroaromatic acids and their derivatives (esters, salts) by carbonylation of the corresponding aryl halides. The acids are selectively formed in a high yield under very mild conditions. Highly active catalytic systems, base-containing alcoholic solutions of cobalt carbonyl modified with epoxides, were used to activate aryl halides. 2005 Pleiades Publishing, Inc.

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