1204956-85-3 Usage
Chemical structure
A benzene ring with four fluorine atoms (F) at positions 1, 2, 4, and 5, and a methoxymethyl group (-OCH2CH3) attached at position 3.
Functional groups
Fluorine atoms, methoxymethyl group
Boiling point
High boiling point due to the presence of fluorine atoms
Melting point
Low to moderate melting point
Density
Higher density compared to similar organic compounds without fluorine atoms
Solubility
Soluble in organic solvents, slightly soluble in water
Stability
Highly resistant to degradation due to the presence of fluorine atoms
Reactivity
Reactive site provided by the methoxymethyl group for further chemical modification
Building block
Used in the synthesis of various organic compounds
Pharmaceutical industry
Potential applications in the development of new drugs
Agrochemicals
Potential use in the development of new pesticides and herbicides
Materials science
Potential use in the development of new materials with unique properties
Versatility
Can be used in a wide range of applications due to its unique properties
Diverse potential uses
Applicable in various industries such as pharmaceuticals, agrochemicals, and materials science
Safety precautions
Handle with care due to its reactivity and potential hazards associated with fluorine-containing compounds. Use appropriate safety measures and personal protective equipment when working with this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 1204956-85-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,4,9,5 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1204956-85:
(9*1)+(8*2)+(7*0)+(6*4)+(5*9)+(4*5)+(3*6)+(2*8)+(1*5)=153
153 % 10 = 3
So 1204956-85-3 is a valid CAS Registry Number.
1204956-85-3Relevant articles and documents
A new synthetic route to polyfluorobenzyl alcohol
Zhang, Deyan,Chen, Zizhan,Cai, Huihua,Zou, Xinzhuo
, p. 938 - 941 (2009)
The synthesis of polyfluorinated benzyl alcohol from pentafluorobenzoic acid has been developed. An economical and effective direct reduction method of polyfluorobenzoic acid by zinc borohydride is described.
