63762-78-7 Usage
Description
2-Fluoro-5-methylanisole (FMA) is an organic compound that is known for its unique properties, which include undergoing copolymerization with other monomers. This characteristic allows it to be a key component in the formation of hydrogels, which have a variety of applications due to their versatile and adaptable nature.
Uses
Used in Ophthalmic Industry:
2-Fluoro-5-methylanisole is used as a copolymerization agent for the creation of hydrogels, which are specifically utilized in the development of ophthalmic lenses. The reason for its use in this application is due to the unique properties of the hydrogels formed, which are beneficial for use in the eye care industry.
The formation of hydrogels through the copolymerization process involving 2-Fluoro-5-methylanisole (FMA) allows for the creation of ophthalmic lenses with enhanced properties. These properties may include improved comfort, durability, and potentially even therapeutic benefits, depending on the specific monomers used in the copolymerization process. The versatility of FMA in forming hydrogels with various monomers makes it a valuable compound in the ophthalmic industry for the development of innovative and improved eye care products.
Check Digit Verification of cas no
The CAS Registry Mumber 63762-78-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,6 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63762-78:
(7*6)+(6*3)+(5*7)+(4*6)+(3*2)+(2*7)+(1*8)=147
147 % 10 = 7
So 63762-78-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H9FO/c1-6-3-4-7(9)8(5-6)10-2/h3-5H,1-2H3
63762-78-7Relevant articles and documents
Synthesis and Dopamine Receptor Affinities of 2-(4-fluoro-3-hydroxyphenyl)ethylamine and N-Substituted Derivatives
Claudi, Francesco,Cardellini, Mario,Cingolani, Gian Mario,Piergentili, Alessandro,Pertuzzi, Guidubaldo,Balduini, Walter
, p. 2408 - 2412 (2007/10/02)
The synthesis of 2-(4-fluoro-3-hydroxyphenyl)ethylamine (26) and of some N,N-dialkyl derivatives (27-30) starting from 4-fluoro-3-hydroxytoluene and their in vitro binding affinities for dopamine (DA) receptor are reported.The amine 26 can be regarded as
Synthesis and evaluation of the antiovulatory activity of a variety of melatonin analogues
Flaugh,Crowell,Clemens,Sawyer
, p. 63 - 69 (2007/10/04)
A series of melatonin analogues was synthesized and examined for ovulation-blocking activity. Deviation from the 5-methoxy group or substitution of the 1 position prevented activity. Activity was not particularly sensitive to minor variations in the N-acyl group nor was it significantly altered by methylation of position 2 or the α-methylene; however, a pronounced enhancement resulted from halogenation of the 6 position.
