Cas 773080-83-4,ethyl (1S,2R,5S,7S,8R,4'S)-7-(2-bromobenzyl)-8-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-2-ethoxy-6-oxotricyclo[3.2.1.0<sup>2,7</sup>]octane-1-carboxylate

773080-83-4

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Product Name: ethyl (1S,2R,5S,7S,8R,4'S)-7-(2-bromobenzyl)-8-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-2-ethoxy-6-oxotricyclo[3.2.1.0^2,7]octane-1-carboxylate
Synonyms: ethyl (1S,2R,5S,7S,8R,4'S)-7-(2-bromobenzyl)-8-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-2-ethoxy-6-oxotricyclo[3.2.1.0^2,7]octane-1-carboxylate
CAS NO:773080-83-4
Molecular Formula:
Molecular Weight: 507.422
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: ethyl (1S,2R,5S,7S,8R,4'S)-7-(2-bromobenzyl)-8-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-2-ethoxy-6-oxotricyclo[3.2.1.0^2,7]octane-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl (1S,2R,5S,7S,8R,4'S)-7-(2-bromobenzyl)-8-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-2-ethoxy-6-oxotricyclo[3.2.1.0^2,7]octane-1-carboxylate(773080-83-4)
EPA Substance Registry System: ethyl (1S,2R,5S,7S,8R,4'S)-7-(2-bromobenzyl)-8-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-2-ethoxy-6-oxotricyclo[3.2.1.0^2,7]octane-1-carboxylate(773080-83-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 773080-83-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 773080-83-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,3,0,8 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 773080-83:
(8*7)+(7*7)+(6*3)+(5*0)+(4*8)+(3*0)+(2*8)+(1*3)=174
174 % 10 = 4
So 773080-83-4 is a valid CAS Registry Number.

773080-83-4Upstream product

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773080-83-4Relevant academic research and scientific papers

One-pot reactions: Enantiomerically pure bicyclo[5.3.1]undecanes; Synthesis of a taxoid compound

Gutke, Hans-Jürgen,Braun, Norbert A.,Spitzner, Dietrich

, p. 8137 - 8141 (2007/10/03)

Reaction of C-2 substituted cyclohexenone with an enantiomerically pure α-bromopentenoate leads to enantiopure tricyclooctane, which can be transformed into a taxoid like compound having the typical bicyclo[5.3.1] undecane skeleton. Graphical Abstract

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