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2,3-Difluoro-6-methoxybenzoyl chloride is a chemical compound with the molecular formula C8H5ClF2O2. It is a derivative of benzoyl chloride, characterized by the presence of two fluorine atoms at the 2nd and 3rd positions and a methoxy group at the 6th position on the benzene ring. 2,3-Difluoro-6-methoxybenzoyl chloride is a clear, colorless liquid with a pungent odor and is highly reactive, readily engaging in reactions with water and alcohols to form corrosive hydrochloric acid. Due to its reactivity and potential health hazards, it is crucial to handle 2,3-Difluoro-6-methoxybenzoyl chloride with care and appropriate protective equipment to prevent skin and eye irritation, respiratory issues, and other adverse effects.

886501-67-3

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886501-67-3 Usage

Uses

Used in Pharmaceutical Industry:
2,3-Difluoro-6-methoxybenzoyl chloride is used as a building block in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it a valuable intermediate for the development of new drugs with specific therapeutic properties. 2,3-Difluoro-6-methoxybenzoyl chloride's ability to form stable bonds with other molecules allows for the creation of complex drug structures with targeted effects on biological systems.
Used in Agrochemical Industry:
In the agrochemical industry, 2,3-Difluoro-6-methoxybenzoyl chloride serves as a key intermediate in the production of various agrochemical compounds, such as pesticides and herbicides. Its reactivity and structural features enable the synthesis of compounds with enhanced efficacy and selectivity, contributing to more effective and environmentally friendly agricultural practices.
Used in Organic Synthesis:
2,3-Difluoro-6-methoxybenzoyl chloride is also utilized in organic synthesis for the preparation of a wide range of organic compounds. Its versatility in forming different types of chemical bonds allows for the creation of diverse molecular structures with various applications in research, industry, and other fields. 2,3-Difluoro-6-methoxybenzoyl chloride's reactivity and stability make it a valuable tool for chemists in designing and synthesizing new organic molecules with specific properties and functions.

Check Digit Verification of cas no

The CAS Registry Mumber 886501-67-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,5,0 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 886501-67:
(8*8)+(7*8)+(6*6)+(5*5)+(4*0)+(3*1)+(2*6)+(1*7)=203
203 % 10 = 3
So 886501-67-3 is a valid CAS Registry Number.

886501-67-3Upstream product

886501-67-3Downstream Products

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