Cas 49611-03-2,N-(6-Methoxy-2-phenyl-quinolin-4-yl)-N'-[1-(5-nitro-furan-2-yl)-meth-(E)-ylidene]-hydrazine

49611-03-2

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Basic information

Product Name: N-(6-Methoxy-2-phenyl-quinolin-4-yl)-N'-[1-(5-nitro-furan-2-yl)-meth-(E)-ylidene]-hydrazine
Synonyms:
CAS NO:49611-03-2
Molecular Formula:
Molecular Weight: 388.382
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: N-(6-Methoxy-2-phenyl-quinolin-4-yl)-N'-[1-(5-nitro-furan-2-yl)-meth-(E)-ylidene]-hydrazine(CAS DataBase Reference)
NIST Chemistry Reference: N-(6-Methoxy-2-phenyl-quinolin-4-yl)-N'-[1-(5-nitro-furan-2-yl)-meth-(E)-ylidene]-hydrazine(49611-03-2)
EPA Substance Registry System: N-(6-Methoxy-2-phenyl-quinolin-4-yl)-N'-[1-(5-nitro-furan-2-yl)-meth-(E)-ylidene]-hydrazine(49611-03-2)

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: 49611-03-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 49611-03-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,1 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 49611-03:
(7*4)+(6*9)+(5*6)+(4*1)+(3*1)+(2*0)+(1*3)=122
122 % 10 = 2
So 49611-03-2 is a valid CAS Registry Number.

49611-03-2Upstream product

698-63-5 5-nitrofurane-2-carboxaldehyde

49611-03-2Downstream Products

49611-03-2Relevant academic research and scientific papers

Synthesis and anti-tubercular evaluation of 4-quinolylhydrazones

Savini, Luisa,Chiasserini, Luisa,Gaeta, Alessandra,Pellerano, Cesare

, p. 2193 - 2198 (2002)

A series of 4-quinolylhydrazones were synthesized and tested against Mycobacterium tuberculosis H37Rv. Preparation of the title compounds was achieved by reaction of 4-quinolylhydrazine and aryl- or heteroaryl-carboxaldehyde. For the most of derivatives interesting antitubercular properties were showed; two compounds (32 and 325), identified as the most active, were tested also against Mycobacterium avium.

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