Cas 114263-11-5,Benzenecarbothioic acid, S-[1-(benzoylphenylamino)-4,4-dicyano-3-(dimethylamino)-1,3-butadien yl] ester

114263-11-5

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Basic information

Product Name: Benzenecarbothioic acid, S-[1-(benzoylphenylamino)-4,4-dicyano-3-(dimethylamino)-1,3-butadien yl] ester
Synonyms:
CAS NO:114263-11-5
Molecular Formula: C28H22N4O2S
Molecular Weight: 478.574
EINECS: N/A
Product Categories: N/A
Mol File: 114263-11-5.mol
Article Data: 1

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: Benzenecarbothioic acid, S-[1-(benzoylphenylamino)-4,4-dicyano-3-(dimethylamino)-1,3-butadien yl] ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzenecarbothioic acid, S-[1-(benzoylphenylamino)-4,4-dicyano-3-(dimethylamino)-1,3-butadien yl] ester(114263-11-5)
EPA Substance Registry System: Benzenecarbothioic acid, S-[1-(benzoylphenylamino)-4,4-dicyano-3-(dimethylamino)-1,3-butadien yl] ester(114263-11-5)

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: 114263-11-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 114263-11-5 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 1 respectively.
Calculate Digit Verification of CAS Registry Number 114263-11:
(8*1)+(7*1)+(6*4)+(5*2)+(4*6)+(3*3)+(2*1)+(1*1)=85
85 % 10 = 5
So 114263-11-5 is a valid CAS Registry Number.

114263-11-5Upstream product

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114263-11-5Relevant articles and documents

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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