850352-73-7 Usage
Uses
Used in Organic Synthesis:
3-Bromo-6,7-dimethoxyquinoline is used as a building block for the synthesis of various pharmaceuticals and biologically active compounds due to its unique structure and reactivity.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-Bromo-6,7-dimethoxyquinoline is utilized as a key intermediate in the development of new drugs, contributing to the creation of complex organic molecules with potential therapeutic applications.
Used in Drug Development:
3-Bromo-6,7-dimethoxyquinoline has been studied for its potential pharmacological properties, indicating its use in the research and development of novel drugs that may offer innovative treatment options for various medical conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 850352-73-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,3,5 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 850352-73:
(8*8)+(7*5)+(6*0)+(5*3)+(4*5)+(3*2)+(2*7)+(1*3)=157
157 % 10 = 7
So 850352-73-7 is a valid CAS Registry Number.
850352-73-7Relevant articles and documents
ANTIMICROBIAL AGENTS
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Page/Page column 135-136, (2012/01/14)
The invention provides a compound of formula I:or a salt thereof, wherein R3-R8 and X and Y have any of the values described in the specification, as well as compositions comprising a compound of formula I. The compounds are useful as antibacterial agents.
Preparation of 1,4-dihydroquinolines bearing a chiral sulfoxide group: New highly enantioselective recyclable NADH mimics
Gaillard, Stéphane,Papamica?l, Cyril,Marsais, Francis,Dupas, Georges,Levacher, Vincent
, p. 441 - 444 (2007/10/03)
The stereoselective preparation of 1-,4-dihydroquinolines possessing a chiral sulfoxide group at C-3 is reported. These novel biomimetic NADH models (R)-1a,b have been shown to be highly enantioselective in the reduction of methyl benzoylformate, producing (R)-methyl mandelate in up to 95% ee. The corresponding quinolinium salts 4a,b have been recovered in good yields. The regenerated models 1a,b could be reused without any significant erosion of the enantioselectivity. Georg Thieme Verlag Stuttgart.
