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484-74-2

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484-74-2 Usage

Description

9-Methylfuro[2,3-b]quinolin-4(9H)-one is a quinolone alkaloid that was initially isolated from the roots of Dictamnus albus and later discovered in Helietta longifoliata. 9-Methylfuro[2,3-b]quinolin-4(9H)-one is characterized by its hygroscopic nature and its tendency to turn red upon exposure to light. It has been confirmed as a true base and not an artifact of isolation through extraction under mild conditions.

Uses

Used in Pharmaceutical Industry:
9-Methylfuro[2,3-b]quinolin-4(9H)-one is used as a pharmaceutical compound for its potential therapeutic applications. Its unique chemical structure and properties make it a candidate for the development of new drugs, particularly in the treatment of various diseases and conditions.
Used in Chemical Research:
In the field of chemical research, 9-Methylfuro[2,3-b]quinolin-4(9H)-one serves as a valuable compound for studying the properties and behavior of quinolone alkaloids. Its hygroscopic nature and light-sensitive characteristics provide insights into the reactivity and stability of similar compounds, contributing to the advancement of chemical knowledge.
Used in Natural Product Extraction:
9-Methylfuro[2,3-b]quinolin-4(9H)-one is used as a marker compound in the extraction and analysis of natural products from plant sources like Dictamnus albus and Helietta longifoliata. Its presence in these plants can help identify and characterize the bioactive components present, which may have potential applications in medicine, agriculture, or other industries.
Used in Material Science:
Due to its light-sensitive properties, 9-Methylfuro[2,3-b]quinolin-4(9H)-one can be utilized in the development of new materials with specific optical or electronic properties. Its ability to change color upon exposure to light may be harnessed for applications in sensors, display technologies, or other optoelectronic devices.

References

Gellert et al., Herb. Hung., 10, 123 (1971) Mammarella, Comin., An. Asoc. Quim. Argentina, 59, 239 (1971)

Check Digit Verification of cas no

The CAS Registry Mumber 484-74-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 4 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 484-74:
(5*4)+(4*8)+(3*4)+(2*7)+(1*4)=82
82 % 10 = 2
So 484-74-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO2/c1-13-10-5-3-2-4-8(10)11(14)9-6-7-15-12(9)13/h2-7H,1H3

484-74-2Downstream Products

484-74-2Relevant articles and documents

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Monkovic et al.

, p. 1935,1946 (1967)

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Studies of heterocyclic compounds. VIII. Synthesis, anti-inflammatory and antiallergic activities of N-alkyl-2,3,4,9-tetrahydrofuro[2,3-b]quinoline-3,4-diones and related compounds

Kuo,Huang,Huang,Cheng,Ling,Wu,Ishii,Nakamura

, p. 955 - 963 (2007/10/02)

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