Cas 185111-93-7,Pyrimido[4,5-d]pyrimidine-2,4(1H,3H)-dione, 5,6,7,8-tetrahydro-1-phenyl-6-(phenylmethyl)-

185111-93-7

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Basic information

Product Name: Pyrimido[4,5-d]pyrimidine-2,4(1H,3H)-dione, 5,6,7,8-tetrahydro-1-phenyl-6-(phenylmethyl)-
Synonyms:
CAS NO:185111-93-7
Molecular Formula: C19H18N4O2
Molecular Weight: 334.378
EINECS: N/A
Product Categories: N/A
Mol File: 185111-93-7.mol

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: Pyrimido[4,5-d]pyrimidine-2,4(1H,3H)-dione, 5,6,7,8-tetrahydro-1-phenyl-6-(phenylmethyl)-(CAS DataBase Reference)
NIST Chemistry Reference: Pyrimido[4,5-d]pyrimidine-2,4(1H,3H)-dione, 5,6,7,8-tetrahydro-1-phenyl-6-(phenylmethyl)-(185111-93-7)
EPA Substance Registry System: Pyrimido[4,5-d]pyrimidine-2,4(1H,3H)-dione, 5,6,7,8-tetrahydro-1-phenyl-6-(phenylmethyl)-(185111-93-7)

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: 185111-93-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 185111-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,5,1,1 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 185111-93:
(8*1)+(7*8)+(6*5)+(5*1)+(4*1)+(3*1)+(2*9)+(1*3)=127
127 % 10 = 7
So 185111-93-7 is a valid CAS Registry Number.

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185111-93-7Relevant academic research and scientific papers

Synthesis, chemical and pharmacological properties of some 2,4-dioxo-1,2,3,4,5,6,7,8-octahydropyrimido [4,5d]pyrimidines

Sladowska,Sieklucka-Dziuba,Rajtar,Wydro,Kleinrok

, p. 39 - 46 (2007/10/03)

Synthesis of 6-substituted 2,4-dioxo-1,2,3,4,5,6,7,8-octahydropyrimido[4,5-d]pyrimidines [III-VI] obtained by cyclocondensation of 1-phenyl-6-aminouracil with formaline and the primary amines is described. Compounds III, V, VI in the Mannich reaction with secondary cyclic amines yield the corresponding 3-substituted N-aminomethyl derivatives VII-X. Some of them were active pharmacologically.

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