Cas 384362-37-2,6-hydroxy-4-oxo-2,4-dihydro-1H-pyrrolo[3,2,1-ij]quinoline-5-carboxylic acid para-metoxyanilide

384362-37-2

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Basic information

Product Name: 6-hydroxy-4-oxo-2,4-dihydro-1H-pyrrolo[3,2,1-ij]quinoline-5-carboxylic acid para-metoxyanilide
Synonyms: 6-hydroxy-4-oxo-2,4-dihydro-1H-pyrrolo[3,2,1-ij]quinoline-5-carboxylic acid para-metoxyanilide
CAS NO:384362-37-2
Molecular Formula:
Molecular Weight: 336.347
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 6-hydroxy-4-oxo-2,4-dihydro-1H-pyrrolo[3,2,1-ij]quinoline-5-carboxylic acid para-metoxyanilide(CAS DataBase Reference)
NIST Chemistry Reference: 6-hydroxy-4-oxo-2,4-dihydro-1H-pyrrolo[3,2,1-ij]quinoline-5-carboxylic acid para-metoxyanilide(384362-37-2)
EPA Substance Registry System: 6-hydroxy-4-oxo-2,4-dihydro-1H-pyrrolo[3,2,1-ij]quinoline-5-carboxylic acid para-metoxyanilide(384362-37-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 384362-37-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 384362-37-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,4,3,6 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 384362-37:
(8*3)+(7*8)+(6*4)+(5*3)+(4*6)+(3*2)+(2*3)+(1*7)=162
162 % 10 = 2
So 384362-37-2 is a valid CAS Registry Number.

384362-37-2Upstream product

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384362-37-2Relevant academic research and scientific papers

4-Hydroxy-2-quinolones 138. Synthesis and study of structure-biological activity relationships in a series of 1-hydroxy-3-oxo-5,6-dihydro-3H-pyrrolo[3, 2,1-ij]quinoline-2-carboxylic acid anilides

Ukrainets,Mospanova,Bereznyakova,Naboka

, p. 1532 - 1539 (2008/12/22)

Two methods are discussed and the synthesis of a series of 1-hydroxy-3-oxo-5,6-dihydro-3H-pyrrolo[3,2,1-ij]quinoline-2-carboxylic acid anilides has been carried out. The antitubercular activity and the effect on the urinary function of the kidney have bee

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