951163-65-8 Usage
Description
Ethanone, 1-(2,4-difluoro-3-hydroxyphenyl)-, also known as 2,4-Difluoro-3-hydroxyacetophenone, is a chemical compound with the formula C8H6F2O2 and a molecular weight of 174.13 g/mol. It is a pale yellow solid with a melting point of 108-111°C and a boiling point of 219-221°C. Ethanone, 1-(2,4-difluoro-3-hydroxyphenyl)is primarily used as an intermediate in the production of various drugs and agrochemicals due to its unique chemical properties. It is considered stable under normal temperatures and pressures, making it suitable for a wide range of applications.
Uses
Used in Pharmaceutical Industry:
Ethanone, 1-(2,4-difluoro-3-hydroxyphenyl)is used as an intermediate in the synthesis of various drugs for its unique chemical properties.
Used in Agrochemical Industry:
Ethanone, 1-(2,4-difluoro-3-hydroxyphenyl)is used as an intermediate in the production of agrochemicals for its unique chemical properties.
Used in Dyes Industry:
Ethanone, 1-(2,4-difluoro-3-hydroxyphenyl)is used as an intermediate in the production of dyes for its unique chemical properties.
Used in Organic Synthesis:
Ethanone, 1-(2,4-difluoro-3-hydroxyphenyl)is used as an intermediate in organic synthesis for its unique chemical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 951163-65-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,1,1,6 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 951163-65:
(8*9)+(7*5)+(6*1)+(5*1)+(4*6)+(3*3)+(2*6)+(1*5)=168
168 % 10 = 8
So 951163-65-8 is a valid CAS Registry Number.
951163-65-8Relevant articles and documents
Coupling process for preparing quinolone intermediates
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Page/Page column 6; 7, (2008/06/13)
Process for making 7-cycloamino-1-cyclopropyl-1,4-dihydro-8-methoxy-4-oxo-3-quinolinecarboxylic acids. Borate ester compounds suitable for use in such process.
Hydride reduction process for preparing quinolone intermediates
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Page/Page column 5-6, (2008/06/13)
Hydride process for making acyclic diol intermediates from cyclic intermediates, useful in antibacterial quinolone synthesis.
