Cas 141040-70-2,(3aR,3bS,8aS,8bS)-2,3,3a,3b,8a,8b-Hexahydro-1H-8-aza-cyclopenta[3,4]cyclobuta[1,2-a]indene-8-carboxylic acid phenyl ester

141040-70-2

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Basic information

Product Name: (3aR,3bS,8aS,8bS)-2,3,3a,3b,8a,8b-Hexahydro-1H-8-aza-cyclopenta[3,4]cyclobuta[1,2-a]indene-8-carboxylic acid phenyl ester
Synonyms:
CAS NO:141040-70-2
Molecular Formula:
Molecular Weight: 305.376
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: (3aR,3bS,8aS,8bS)-2,3,3a,3b,8a,8b-Hexahydro-1H-8-aza-cyclopenta[3,4]cyclobuta[1,2-a]indene-8-carboxylic acid phenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (3aR,3bS,8aS,8bS)-2,3,3a,3b,8a,8b-Hexahydro-1H-8-aza-cyclopenta[3,4]cyclobuta[1,2-a]indene-8-carboxylic acid phenyl ester(141040-70-2)
EPA Substance Registry System: (3aR,3bS,8aS,8bS)-2,3,3a,3b,8a,8b-Hexahydro-1H-8-aza-cyclopenta[3,4]cyclobuta[1,2-a]indene-8-carboxylic acid phenyl ester(141040-70-2)

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: 141040-70-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141040-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,4 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 141040-70:
(8*1)+(7*4)+(6*1)+(5*0)+(4*4)+(3*0)+(2*7)+(1*0)=72
72 % 10 = 2
So 141040-70-2 is a valid CAS Registry Number.

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141040-70-2Relevant academic research and scientific papers

Removable groups for activation of indole photochemistry

Weedon,Zhang

, p. 95 - 100 (1992)

The ability of a series of nitrogen-substituents to activate the cycloaddition photochemistry of indoles has been examined; the N-substitutents were chosen in order to enable their removal following cycloaddition under mild neutral, acidic or basic condit

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