Cas 132127-75-4,(5R,6R)-5,6-Diallyl-7-oxo-5-(3,4,5-trimethoxy-phenyl)-6,7-dihydro-5H-indeno[5,6-d][1,3]dioxole-6-carboxylic acid methyl ester

132127-75-4

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Basic information

Product Name: (5R,6R)-5,6-Diallyl-7-oxo-5-(3,4,5-trimethoxy-phenyl)-6,7-dihydro-5H-indeno[5,6-d][1,3]dioxole-6-carboxylic acid methyl ester
Synonyms:
CAS NO:132127-75-4
Molecular Formula:
Molecular Weight: 480.515
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: (5R,6R)-5,6-Diallyl-7-oxo-5-(3,4,5-trimethoxy-phenyl)-6,7-dihydro-5H-indeno[5,6-d][1,3]dioxole-6-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (5R,6R)-5,6-Diallyl-7-oxo-5-(3,4,5-trimethoxy-phenyl)-6,7-dihydro-5H-indeno[5,6-d][1,3]dioxole-6-carboxylic acid methyl ester(132127-75-4)
EPA Substance Registry System: (5R,6R)-5,6-Diallyl-7-oxo-5-(3,4,5-trimethoxy-phenyl)-6,7-dihydro-5H-indeno[5,6-d][1,3]dioxole-6-carboxylic acid methyl ester(132127-75-4)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 132127-75-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 132127-75-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,1,2 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 132127-75:
(8*1)+(7*3)+(6*2)+(5*1)+(4*2)+(3*7)+(2*7)+(1*5)=94
94 % 10 = 4
So 132127-75-4 is a valid CAS Registry Number.

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132127-75-4Relevant academic research and scientific papers

Synthesis and Antitumor Activity of Structural Analogues of the Epipodophyllotoxins

Klein, Larry L.,Yeung, Clinton M.,Chu, Daniel T.,McDonald, Edith J.,Clement, Jacob J.,Plattner, Jacob J.

, p. 984 - 992 (2007/10/02)

Several ring-contracted analogues of the antitumor agent etoposide have been prepared.The synthesis of the simple indanyl system 3 is described along with two bicyclic systems of general structure 4 prepared through a stereoselective allylation of the ket

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