Cas 75832-17-6,(2S,3aR,7aR)-1-Benzyl-2,3,3a,7a-tetrahydro-1H-indole-2,4,6,7-tetracarboxylic acid tetramethyl ester

75832-17-6

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Basic information

Product Name: (2S,3aR,7aR)-1-Benzyl-2,3,3a,7a-tetrahydro-1H-indole-2,4,6,7-tetracarboxylic acid tetramethyl ester
Synonyms:
CAS NO:75832-17-6
Molecular Formula:
Molecular Weight: 443.453
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,3aR,7aR)-1-Benzyl-2,3,3a,7a-tetrahydro-1H-indole-2,4,6,7-tetracarboxylic acid tetramethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3aR,7aR)-1-Benzyl-2,3,3a,7a-tetrahydro-1H-indole-2,4,6,7-tetracarboxylic acid tetramethyl ester(75832-17-6)
EPA Substance Registry System: (2S,3aR,7aR)-1-Benzyl-2,3,3a,7a-tetrahydro-1H-indole-2,4,6,7-tetracarboxylic acid tetramethyl ester(75832-17-6)

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: 75832-17-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 75832-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,3 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 75832-17:
(7*7)+(6*5)+(5*8)+(4*3)+(3*2)+(2*1)+(1*7)=146
146 % 10 = 6
So 75832-17-6 is a valid CAS Registry Number.

75832-17-6Upstream product

75832-17-6Downstream Products

75817-91-3 1-Benzyl-1H-indole-2,4,6,7-tetracarboxylic acid tetramethyl ester

75832-17-6Relevant academic research and scientific papers

Electrophilic reactions of DMAD with a cyclic dienamine: Solvent influence upon the competitive formation of [4+2]-,[2+2]- and michael type adducts

Eberbach, Wolfgang,Claude Carre, Jean

, p. 1145 - 1148 (2007/10/02)

The reaction course of DMAD with dihydroazepine 3 depends strongly on the solvent: under appropriate conditions either 4, 5 or 6(E) is formed as the exclusive addition product.

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