Cas 192653-62-6,1H-Pyrrole-2-carboxylic acid, 3-[[bis(benzoylamino)methylene]amino]-4-(3-pyridinylmethyl)-, methyl ester

192653-62-6

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Basic information

Product Name: 1H-Pyrrole-2-carboxylic acid, 3-[[bis(benzoylamino)methylene]amino]-4-(3-pyridinylmethyl)-, methyl ester
Synonyms:
CAS NO:192653-62-6
Molecular Formula: C27H23N5O4
Molecular Weight: 481.511
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: 1H-Pyrrole-2-carboxylic acid, 3-[[bis(benzoylamino)methylene]amino]-4-(3-pyridinylmethyl)-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1H-Pyrrole-2-carboxylic acid, 3-[[bis(benzoylamino)methylene]amino]-4-(3-pyridinylmethyl)-, methyl ester(192653-62-6)
EPA Substance Registry System: 1H-Pyrrole-2-carboxylic acid, 3-[[bis(benzoylamino)methylene]amino]-4-(3-pyridinylmethyl)-, methyl ester(192653-62-6)

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: 192653-62-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 192653-62-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,6,5 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 192653-62:
(8*1)+(7*9)+(6*2)+(5*6)+(4*5)+(3*3)+(2*6)+(1*2)=156
156 % 10 = 6
So 192653-62-6 is a valid CAS Registry Number.

192653-62-6Upstream product

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192653-62-6Relevant academic research and scientific papers

Process for the preparation of 9-deazaguanine derivatives

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Page 20, (2010/02/09)

Derivatives of 9-deazaguanine are prepared by reacting an aldehyde or ketone with a dialkylaminomalonate to form the corresponding enamine. The enamine is then reacted with a base to form a cyclic pyrrole. The cyclic pyrrole is reacted with an urea compound or a derivative of carbamimidoic acid to provide a protected guanidino compound. The guanidino is converted to the desired 9-deazaguanine derivative by reacting with trifluoracetic acid or with an alkoxide or hydroxide followed by neutralization with an acid.

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