Cas 1070802-29-7,5-{(anilino)[(octahydro-2H-quinolizin-1-ylmethyl)amino]methylidene}-1,3-dicyclohexylpyrimidine-2,4,6(1H,3H,5H)-trione

1070802-29-7

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Basic information

Product Name: 5-{(anilino)[(octahydro-2H-quinolizin-1-ylmethyl)amino]methylidene}-1,3-dicyclohexylpyrimidine-2,4,6(1H,3H,5H)-trione
Synonyms:
CAS NO:1070802-29-7
Molecular Formula:
Molecular Weight: 561.768
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: 5-{(anilino)[(octahydro-2H-quinolizin-1-ylmethyl)amino]methylidene}-1,3-dicyclohexylpyrimidine-2,4,6(1H,3H,5H)-trione(CAS DataBase Reference)
NIST Chemistry Reference: 5-{(anilino)[(octahydro-2H-quinolizin-1-ylmethyl)amino]methylidene}-1,3-dicyclohexylpyrimidine-2,4,6(1H,3H,5H)-trione(1070802-29-7)
EPA Substance Registry System: 5-{(anilino)[(octahydro-2H-quinolizin-1-ylmethyl)amino]methylidene}-1,3-dicyclohexylpyrimidine-2,4,6(1H,3H,5H)-trione(1070802-29-7)

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1070802-29-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1070802-29-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,0,8,0 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1070802-29:
(9*1)+(8*0)+(7*7)+(6*0)+(5*8)+(4*0)+(3*2)+(2*2)+(1*9)=117
117 % 10 = 7
So 1070802-29-7 is a valid CAS Registry Number.

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1070802-29-7Relevant academic research and scientific papers

A new method for the synthesis of 5-amidinobarbiturates

Paramonov,Belyaev,Bakulev

, p. 1617 - 1623 (2008/09/18)

The reactions of 5-[arylamino(methylthio)methylene]pyrimidine-2,4,6(1H,3H, 5H)-triones with different aliphatic and aromatic amines were studied. A series of 5-amidinobarbiturates was synthesized. A new and preparatively convenient method for their synthesis appropriate for the use in the combinatorial chemistry was developed.

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