Cas 1020169-93-0,2-(1-benzhydryl-2-tert-butoxycarbonyl-2,3-dihydro-1H-indol-3-yl)-2-benzyl-malonic acid diethyl ester

1020169-93-0

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Basic information

Product Name: 2-(1-benzhydryl-2-tert-butoxycarbonyl-2,3-dihydro-1H-indol-3-yl)-2-benzyl-malonic acid diethyl ester
Synonyms: 2-(1-benzhydryl-2-tert-butoxycarbonyl-2,3-dihydro-1H-indol-3-yl)-2-benzyl-malonic acid diethyl ester
CAS NO:1020169-93-0
Molecular Formula:
Molecular Weight: 633.785
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: 2-(1-benzhydryl-2-tert-butoxycarbonyl-2,3-dihydro-1H-indol-3-yl)-2-benzyl-malonic acid diethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-(1-benzhydryl-2-tert-butoxycarbonyl-2,3-dihydro-1H-indol-3-yl)-2-benzyl-malonic acid diethyl ester(1020169-93-0)
EPA Substance Registry System: 2-(1-benzhydryl-2-tert-butoxycarbonyl-2,3-dihydro-1H-indol-3-yl)-2-benzyl-malonic acid diethyl ester(1020169-93-0)

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: 1020169-93-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1020169-93-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,0,1,6 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1020169-93:
(9*1)+(8*0)+(7*2)+(6*0)+(5*1)+(4*6)+(3*9)+(2*9)+(1*3)=100
100 % 10 = 0
So 1020169-93-0 is a valid CAS Registry Number.

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1020169-93-0Relevant academic research and scientific papers

Free radical-mediated aryl amination: Convergent two- and three-component couplings to chiral 2,3-disubstituted indolines

Viswanathan, Rajesh,Smith, Colin R.,Prabhakaran, Erode N.,Johnston, Jeffrey N.

, p. 3040 - 3046 (2008)

(Chemical Equation Presented) 5-exo-trig Cyclization of an aryl radical to the nitrogen of an azomethine is used as the key annulating step in a modular preparation of 2,3-cis- and trans-disubstituted indolines. The precursors are readily prepared by phas

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