2255-50-7 Usage
Description
4-Methoxyfuro[2,3-b]quinolin-8-ol is a quinoline alkaloid derived from Haplophyllum robustum Bge., which forms colorless crystals from ethanol. It is characterized by the presence of a methoxy and a hydroxy group at positions 4 and 8, respectively, on the furo[2,3-b]quinoline structure. This alkaloid has the ability to form a series of crystalline salts and derivatives, including the hydrochloride, picrate, acetyl derivative, methyl derivative, and the tetrahydro compound.
Uses
Used in Pharmaceutical Industry:
4-Methoxyfuro[2,3-b]quinolin-8-ol is used as a pharmaceutical compound for its potential therapeutic applications. The expression is: 4-Methoxyfuro[2,3-b]quinolin-8-ol is used as a therapeutic agent for its alkaloid properties and potential medicinal benefits.
Used in Chemical Research:
In the field of chemical research, 4-Methoxyfuro[2,3-b]quinolin-8-ol serves as a valuable compound for studying the structure and properties of quinoline alkaloids. The expression is: 4-Methoxyfuro[2,3-b]quinolin-8-ol is used as a research compound for understanding the chemical behavior and potential applications of quinoline alkaloids.
Used in Drug Synthesis:
4-Methoxyfuro[2,3-b]quinolin-8-ol can be utilized as a key intermediate in the synthesis of various drugs and pharmaceuticals. The expression is: 4-Methoxyfuro[2,3-b]quinolin-8-ol is used as a synthetic intermediate for the development of new drugs and pharmaceuticals.
Used in Material Science:
The unique properties of 4-Methoxyfuro[2,3-b]quinolin-8-ol, such as its ability to form crystalline salts and derivatives, make it a potential candidate for applications in material science. The expression is: 4-Methoxyfuro[2,3-b]quinolin-8-ol is used as a material component for exploring its potential in various material science applications.
References
Fakhritdinova, Sidyakin, Yunusov,Khim. Prir.Soedin., 1, 107 (1965) Faizutdinova, Yunusov, ibid, 3, 260 (1967) Narasimhan, Paradkar, Alurkar, Tetrahedron, 27,1351 (1971)
Check Digit Verification of cas no
The CAS Registry Mumber 2255-50-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,5 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2255-50:
(6*2)+(5*2)+(4*5)+(3*5)+(2*5)+(1*0)=67
67 % 10 = 7
So 2255-50-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO3/c1-15-11-7-3-2-4-9(14)10(7)13-12-8(11)5-6-16-12/h2-6,14H,1H3
2255-50-7Relevant articles and documents
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Abdullaeva,Kh.A. et al.
, (1978)
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cis-dihydrodiol, arene oxide and phenol metabolites of dictamnine: Key intermediates in the biodegradation and biosynthesis of furoquinoline alkaloids
Boyd, Derek R.,Sharma, Narain D.,O'Dowd, Colin R.,Carroll, Jonathan G.,Loke, Pui L.,Allen, Christopher C. R.
, p. 3989 - 3991 (2007/10/03)
Biotransformation of the parent furoquinoline alkaloid dictamnine and its 4-chlorofuroquinoline precursor, using the B8/ 36 bacterial mutant strain of Sphingomonas yanoikuyae, yielded, via biphenyl dioxygenase-catalysed dihydroxylation, the first isolable alkaloid cis-dihydrodiol metabolites; these metabolites were used in the chemoenzymatic synthesis of postulated arene oxide and phenol intermediates, and a range of derived furoquinoline alkaloids. The Royal Society of Chemistry 2005.
