Cas 133828-95-2,(2S,3S,8aR)-3-Carbamoyl-1,6-dicyano-2-(4-fluoro-phenyl)-1,2,3,8a-tetrahydro-indolizine-1-carboxylic acid ethyl ester

133828-95-2

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Basic information

Product Name: (2S,3S,8aR)-3-Carbamoyl-1,6-dicyano-2-(4-fluoro-phenyl)-1,2,3,8a-tetrahydro-indolizine-1-carboxylic acid ethyl ester
Synonyms:
CAS NO:133828-95-2
Molecular Formula:
Molecular Weight: 380.378
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: (2S,3S,8aR)-3-Carbamoyl-1,6-dicyano-2-(4-fluoro-phenyl)-1,2,3,8a-tetrahydro-indolizine-1-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S,8aR)-3-Carbamoyl-1,6-dicyano-2-(4-fluoro-phenyl)-1,2,3,8a-tetrahydro-indolizine-1-carboxylic acid ethyl ester(133828-95-2)
EPA Substance Registry System: (2S,3S,8aR)-3-Carbamoyl-1,6-dicyano-2-(4-fluoro-phenyl)-1,2,3,8a-tetrahydro-indolizine-1-carboxylic acid ethyl ester(133828-95-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 133828-95-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 133828-95-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,8,2 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 133828-95:
(8*1)+(7*3)+(6*3)+(5*8)+(4*2)+(3*8)+(2*9)+(1*5)=142
142 % 10 = 2
So 133828-95-2 is a valid CAS Registry Number.

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133828-95-2Relevant academic research and scientific papers

Regio- and stereoselective synthesis of tetrahydroindolysines, tetrahydropyridin-6-olates, and cyclopropanes from pyridinium ylides and unsaturated nitriles

Shestopalov,Litvinov,Rodinovskaya,Sharanin

, p. 129 - 138 (2007/10/02)

The regio- and stereoselectivity of the reactions of pyridinium ylides with unsaturated nitriles are dependent on the electronic nature of the substituent in position 3 of the pyridine ring. The reaction of 1-carbamoylmethylide-3-cyanopyridinium with aryl

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