Cas 1408005-91-3,6-(4-fluorophenyl)-1,3-dimethyl-5-(2-oxoindolin-3-yl)-1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dione

1408005-91-3

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Basic information

Product Name: 6-(4-fluorophenyl)-1,3-dimethyl-5-(2-oxoindolin-3-yl)-1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dione
Synonyms: 6-(4-fluorophenyl)-1,3-dimethyl-5-(2-oxoindolin-3-yl)-1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dione
CAS NO:1408005-91-3
Molecular Formula:
Molecular Weight: 404.4
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-(4-fluorophenyl)-1,3-dimethyl-5-(2-oxoindolin-3-yl)-1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: 6-(4-fluorophenyl)-1,3-dimethyl-5-(2-oxoindolin-3-yl)-1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dione(1408005-91-3)
EPA Substance Registry System: 6-(4-fluorophenyl)-1,3-dimethyl-5-(2-oxoindolin-3-yl)-1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dione(1408005-91-3)

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: 1408005-91-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1408005-91-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,8,0,0 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1408005-91:
(9*1)+(8*4)+(7*0)+(6*8)+(5*0)+(4*0)+(3*5)+(2*9)+(1*1)=123
123 % 10 = 3
So 1408005-91-3 is a valid CAS Registry Number.

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1408005-91-3Relevant academic research and scientific papers

Synthesis of novel oxindolylpyrrolo[2,3-d]pyrimidines via a three-component sequential tandem reaction

Rad-Moghadam, Kurosh,Azimi, Seyyedeh Cobra

, p. 9706 - 9712 (2012/11/07)

A novel one-pot three-component reaction of 6-amino-uracil, isatin, and acetophenone was accomplished through a programmed pH variation for the synthesis of 5-(2-oxoindolin-3-yl)-1H-pyrrolo[2,3-d]pyrimidine-2,4(3H,7H)-dione derivatives. The reaction was c

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