Cas 73233-08-6,(1S,3aR,4S,6R,7S,7aS)-4-Acetoxy-7a-hydroxy-1,3,3,6-tetramethyl-octahydro-indene-1,7-dicarboxylic acid dimethyl ester

73233-08-6

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Basic information

Product Name: (1S,3aR,4S,6R,7S,7aS)-4-Acetoxy-7a-hydroxy-1,3,3,6-tetramethyl-octahydro-indene-1,7-dicarboxylic acid dimethyl ester
Synonyms: (1S,3aR,4S,6R,7S,7aS)-4-Acetoxy-7a-hydroxy-1,3,3,6-tetramethyl-octahydro-indene-1,7-dicarboxylic acid dimethyl ester
CAS NO:73233-08-6
Molecular Formula:
Molecular Weight: 370.443
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: (1S,3aR,4S,6R,7S,7aS)-4-Acetoxy-7a-hydroxy-1,3,3,6-tetramethyl-octahydro-indene-1,7-dicarboxylic acid dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1S,3aR,4S,6R,7S,7aS)-4-Acetoxy-7a-hydroxy-1,3,3,6-tetramethyl-octahydro-indene-1,7-dicarboxylic acid dimethyl ester(73233-08-6)
EPA Substance Registry System: (1S,3aR,4S,6R,7S,7aS)-4-Acetoxy-7a-hydroxy-1,3,3,6-tetramethyl-octahydro-indene-1,7-dicarboxylic acid dimethyl ester(73233-08-6)

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: 73233-08-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 73233-08-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,2,3 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73233-08:
(7*7)+(6*3)+(5*2)+(4*3)+(3*3)+(2*0)+(1*8)=106
106 % 10 = 6
So 73233-08-6 is a valid CAS Registry Number.

73233-08-6Upstream product

54986-75-3 dihydrobotrydial

73233-08-6Downstream Products

73233-08-6Relevant academic research and scientific papers

Chemical transformations on botryane skeleton. Effect on the cytotoxic activity

Reino, Jose L.,Duran-Patron, Rosa,Segura, Inmaculada,Hernandez-Galan, Rosario,Riese, Hans H.,Collado, Isidro G.

, p. 344 - 349 (2007/10/03)

Eighteen compounds with a botryane skeleton have been obtained through chemical transformations of various toxins from the fungus Botrytis cinerea. During the course of these transformations, the C-10 carbon of the botryane skeleton was found to exhibit an interesting high regioselectivity to oxidizing and reducing agents. In addition, the cytotoxicity of 27 botryane derivatives was determined in vitro against Hs578T, MDA-MB-231, HT-1080, U87-MG, IMR-90, and HUVEC cell lines. The results of this study confirm that the cytotoxicity of botrydial (1) and its derivatives is related to the presence of a 1,5-dialdehyde functionality.

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