2375-90-8 Usage
Description
CHEMBRDG-BB 5563067 is a poly(ethylene glycol) derivative, a chemical compound with the systematic name 2-(5-[4-(Ethoxycarbonylmethoxy)phenyl]-4-oxo-4H-pyran-2-yloxy)ethyl methyl(2E)-3-phenylprop-2-enoate. It is known for its solubility in water and potential applications in pharmaceutical and biotechnological fields.
Uses
Used in Pharmaceutical Industry:
CHEMBRDG-BB 5563067 is used as a drug delivery vehicle for enhancing the solubility, stability, and bioavailability of therapeutic agents.
Used in Biotechnological Applications:
CHEMBRDG-BB 5563067 is used as a coating material for medical devices to improve their biocompatibility and reduce the risk of adverse reactions.
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.