2375-90-8 Usage
General Description
CHEMBRDG-BB 5563067 is a chemical compound that is classified under the category of poly(ethylene glycol) derivatives. It is also known by its systematic name, 2-({5-[4-(Ethoxycarbonylmethoxy)phenyl]-4-oxo-4H-pyran-2-yl}oxy)ethyl methyl(2E)-3-phenylprop-2-enoate. CHEMBRDG-BB 5563067 is a derivative of poly(ethylene glycol), a commonly used polymer in various pharmaceutical and biotechnological applications. CHEMBRDG-BB 5563067 is likely to have properties and uses similar to those of poly(ethylene glycol), such as its solubility in water and its potential as a drug delivery vehicle or coating material for medical devices. However, specific information regarding its uses, properties, and potential hazards is not readily available.
Check Digit Verification of cas no
The CAS Registry Mumber 2375-90-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,7 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2375-90:
(6*2)+(5*3)+(4*7)+(3*5)+(2*9)+(1*0)=88
88 % 10 = 8
So 2375-90-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H3F4NO/c1-12-4-2(7)5(9)11-6(10)3(4)8/h1H3
2375-90-8Relevant articles and documents
Banks, R. E.,Field, D. S.,Haszeldine, R. N.
, p. 1822 - 1826 (1967)
Benzamidine derivatives and their use as anti-coagulants
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Page column 33, (2010/02/04)
This invention is directed to benzamidine derivatives which are useful as anti-coagulants. This invention is also directed to pharmaceutical compositions containing the compounds of the invention, and methods of using the compounds to treat disease-states characterized by thrombotic activity.
MECHANISMS FOR REACTIONS OF HALOGENATED COMPOUNDS. PART 6. INVESTIGATIONS INTO THE ACTIVATING EFFECT OF ORTHO-FLUORINE IN NUCLEOPHILIC AROMATIC SUBSTITUTION
Chambers, Richard D.,Seabury, Mark J.,Williams, D. Lyn H.,Hughes, Nigel
, p. 255 - 258 (2007/10/02)
Separate activating effects for ortho- and meta- fluorine, on nucleophilic aromatic substitution, are determinated for pyrimidine and pyridine systems.Comparisons confirm the importance of ion-dipole interactions for activation by ortho-fluorine.The effects of ortho-fluorine on anionic ?-complexes are also discussed.
