Cas 1078713-91-3,(S)-tert-butyl 2-(2-(4-methylphenylsulfonamido)ethyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate

1078713-91-3

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Basic information

Product Name: (S)-tert-butyl 2-(2-(4-methylphenylsulfonamido)ethyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate
Synonyms: (S)-tert-butyl 2-(2-(4-methylphenylsulfonamido)ethyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate
CAS NO:1078713-91-3
Molecular Formula:
Molecular Weight: 459.563
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: (S)-tert-butyl 2-(2-(4-methylphenylsulfonamido)ethyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-tert-butyl 2-(2-(4-methylphenylsulfonamido)ethyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate(1078713-91-3)
EPA Substance Registry System: (S)-tert-butyl 2-(2-(4-methylphenylsulfonamido)ethyl)-1-oxo-2,3-dihydro-1H-indene-2-carboxylate(1078713-91-3)

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: 1078713-91-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1078713-91-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,8,7,1 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1078713-91:
(9*1)+(8*0)+(7*7)+(6*8)+(5*7)+(4*1)+(3*3)+(2*9)+(1*1)=173
173 % 10 = 3
So 1078713-91-3 is a valid CAS Registry Number.

1078713-91-3Upstream product

1078713-91-3Downstream Products

1078713-91-3Relevant academic research and scientific papers

Organocatalytic asymmetric ring-opening of aziridines

Paixao, Marcio W.,Nielsen, Martin,Jacobsen, Christian Borch,Jorgensen, Karl Anker

supporting information; experimental part, p. 3467 - 3470 (2009/02/05)

The organocatalytic ring-opening of N-tosyl protected aziridines by β-ketoesters under chiral PTC-conditions, leading to the formation of optically active aminoethyl functionalised compounds with up to 99% ee, has been developed.

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