Cas 114263-10-4,3-Pyridinecarbonitrile, 2-amino-4-(dimethylamino)-1,6-dihydro-1,5-bis(phenylmethyl)-6-thioxo-

114263-10-4

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Basic information

Product Name: 3-Pyridinecarbonitrile, 2-amino-4-(dimethylamino)-1,6-dihydro-1,5-bis(phenylmethyl)-6-thioxo-
Synonyms:
CAS NO:114263-10-4
Molecular Formula: C22H22N4S
Molecular Weight: 374.509
EINECS: N/A
Product Categories: N/A
Mol File: 114263-10-4.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: 3-Pyridinecarbonitrile, 2-amino-4-(dimethylamino)-1,6-dihydro-1,5-bis(phenylmethyl)-6-thioxo-(CAS DataBase Reference)
NIST Chemistry Reference: 3-Pyridinecarbonitrile, 2-amino-4-(dimethylamino)-1,6-dihydro-1,5-bis(phenylmethyl)-6-thioxo-(114263-10-4)
EPA Substance Registry System: 3-Pyridinecarbonitrile, 2-amino-4-(dimethylamino)-1,6-dihydro-1,5-bis(phenylmethyl)-6-thioxo-(114263-10-4)

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: 114263-10-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 114263-10-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,2,6 and 3 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 114263-10:
(8*1)+(7*1)+(6*4)+(5*2)+(4*6)+(3*3)+(2*1)+(1*0)=84
84 % 10 = 4
So 114263-10-4 is a valid CAS Registry Number.

114263-10-4Upstream product

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114263-10-4Relevant academic research and scientific papers

Ketene-S,N-acetals as Synthetic Intermediates for Heterocycles. New Synthesis of Multisubstituted Pyridine-2-thiones

Takahata, Hiroki,Wang, Eng-Chi,Nakajima, Tomoko,Yamazaki, Takao

, p. 3139 - 3145 (2007/10/02)

Ketene-S,N-acetals reacted with isothiocyanates to give β-aminothiocarbonyl-α-methylthioenamines, which were transformed into enaminonitriles by carbon-carbon bond formation with malononitriles.Treatment of the enaminonitriles with base afforded pyridine-

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