Cas 917496-16-3,2-{[7-(3-chloro-4-fluoro-phenyl)-5-phenyl-7<i>H</i>-pyrrolo[2,3-<i>d</i>]pyrimidin-4-ylamino]-methylene}-malonic acid diethyl ester

917496-16-3

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Basic information

Product Name: 2-{[7-(3-chloro-4-fluoro-phenyl)-5-phenyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino]-methylene}-malonic acid diethyl ester
Synonyms:
CAS NO:917496-16-3
Molecular Formula:
Molecular Weight: 508.936
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: 2-{[7-(3-chloro-4-fluoro-phenyl)-5-phenyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino]-methylene}-malonic acid diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-{[7-(3-chloro-4-fluoro-phenyl)-5-phenyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino]-methylene}-malonic acid diethyl ester(917496-16-3)
EPA Substance Registry System: 2-{[7-(3-chloro-4-fluoro-phenyl)-5-phenyl-7H-pyrrolo[2,3-d]pyrimidin-4-ylamino]-methylene}-malonic acid diethyl ester(917496-16-3)

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: 917496-16-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 917496-16-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,7,4,9 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 917496-16:
(8*9)+(7*1)+(6*7)+(5*4)+(4*9)+(3*6)+(2*1)+(1*6)=203
203 % 10 = 3
So 917496-16-3 is a valid CAS Registry Number.

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917496-16-3Relevant academic research and scientific papers

The Gould-Jacob type of reaction for the synthesis of novel pyrimidopyrrolopyrimidines: A comparison of classical heating vs solvent free microwave irradiation

Desai, Nirmal D.

, p. 1343 - 1348 (2007/10/03)

The Gould-Jacob type of reaction for the synthesis of ethyl 4-oxo-8,10-substituted-4,8-dihydropyrimido[1,2-c]pyrrolo[3,2-e] pyrimidine-3-carboxylates 5 has been carried out conventionally by the condensation between 4-aminopyrrolo[2,3-d]pyrimidines 2 and

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