Cas 1144031-16-2,methyl 7-chloro-9-oxo-3-(phenylhydrazono)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazoline-1-carboxylate

1144031-16-2

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Basic information

Product Name: methyl 7-chloro-9-oxo-3-(phenylhydrazono)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazoline-1-carboxylate
Synonyms: methyl 7-chloro-9-oxo-3-(phenylhydrazono)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazoline-1-carboxylate
CAS NO:1144031-16-2
Molecular Formula:
Molecular Weight: 382.806
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: methyl 7-chloro-9-oxo-3-(phenylhydrazono)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazoline-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 7-chloro-9-oxo-3-(phenylhydrazono)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazoline-1-carboxylate(1144031-16-2)
EPA Substance Registry System: methyl 7-chloro-9-oxo-3-(phenylhydrazono)-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazoline-1-carboxylate(1144031-16-2)

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: 1144031-16-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1144031-16-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,4,0,3 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1144031-16:
(9*1)+(8*1)+(7*4)+(6*4)+(5*0)+(4*3)+(3*1)+(2*1)+(1*6)=92
92 % 10 = 2
So 1144031-16-2 is a valid CAS Registry Number.

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1144031-16-2Relevant academic research and scientific papers

Toward new camptothecins. Part 5: On the synthesis of precursors for the crucial Friedl?nder reaction

Boisse, Thomas,Gavara, Laurent,Hénichart, Jean-Pierre,Rigo, Beno?t,Gautret, Philippe

, p. 2455 - 2466 (2009)

The synthesis of potential precursors of ketones, which could be used to obtain camptothecin analogs, is described. Noteworthy is the difference of reactivity between indolizinone and pyrrolidinoquinazolinone heterocycle.

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