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5-BROMO-2-(DIFLUOROMETHOXY)BENZALDEHYD, a chemical compound with the molecular formula C8H5BrF2O2, is a white crystalline solid. It has a molecular weight of 251.03 g/mol and is recognized for its versatile reactivity in organic synthesis and medicinal chemistry research. 5-BROMO-2-(DIFLUOROMETHOXY)BENZALDEHYD is valued for its ability to introduce fluorine-containing functional groups into organic molecules, which is crucial for enhancing the properties of various pharmaceuticals and agrochemicals.

329269-64-9

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329269-64-9 Usage

Uses

Used in Pharmaceutical Industry:
5-BROMO-2-(DIFLUOROMETHOXY)BENZALDEHYD is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of novel bioactive compounds. Its incorporation into drug molecules can improve their efficacy, selectivity, and pharmacokinetic properties, making it a valuable tool in drug discovery and development.
Used in Agrochemical Industry:
In the agrochemical sector, 5-BROMO-2-(DIFLUOROMETHOXY)BENZALDEHYD is utilized as an intermediate in the production of agrochemicals. Its role in introducing fluorine-containing functional groups can enhance the performance of these chemicals, potentially increasing their effectiveness in pest control and crop protection.
Used in Organic Synthesis:
5-BROMO-2-(DIFLUOROMETHOXY)BENZALDEHYD is employed as a versatile building block in organic synthesis. Its reactivity allows for the creation of a wide range of organic molecules, which can be tailored for specific applications in various industries.
Used in Medicinal Chemistry Research:
As a key component in medicinal chemistry research, 5-BROMO-2-(DIFLUOROMETHOXY)BENZALDEHYD is used to explore new chemical entities and optimize existing drug candidates. Its introduction of fluorine-containing groups can significantly impact the pharmacological profile of molecules, leading to improved therapeutic agents.
Used in Fine Chemicals Industry:
In the fine chemicals industry, 5-BROMO-2-(DIFLUOROMETHOXY)BENZALDEHYD is utilized for the synthesis of specialty chemicals that have specific applications in various fields, such as fragrances, dyes, and high-performance materials. Its unique properties make it an essential component in the development of these high-value products.

Check Digit Verification of cas no

The CAS Registry Mumber 329269-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,2,6 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 329269-64:
(8*3)+(7*2)+(6*9)+(5*2)+(4*6)+(3*9)+(2*6)+(1*4)=169
169 % 10 = 9
So 329269-64-9 is a valid CAS Registry Number.

329269-64-9SDS

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 5-Bromo-2-(difluoromethoxy)benzaldehyde

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:329269-64-9 SDS

329269-64-9Upstream product

329269-64-9Relevant academic research and scientific papers

Difluoromethylation of Phenols and Thiophenols with the S-(Difluo-romethyl)sulfonium Salt: Reaction, Scope, and Mechanistic Study

Liu, Guo-Kai,Qin, Wen-Bing,Li, Xin,Lin, Li-Ting,Wong, Henry N. C.

, p. 15948 - 15957 (2019)

A facile and practical approach for the difluoromethylation of phenols and thiophenols was described. Making use of the recently developed bench-stable S-(difluoromethyl)sulfonium salt as the difluorocarbene precursor, a wide variety of diversely functionalized phenols and thiophenols were readily converted to their corresponding aryl difluoromethyl ethers in good to excellent yields in the presence of lithium hydroxide. Chemoselectivity of various O,S-nucleophiles toward difluorocarbene was systematically studied, suggesting the reactivity order ArS- > RS-, ArO- > ROH > RO-, ArSH, ArOH, RSH.

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