Cas 82134-64-3,4-Bromo-benzoic acid (R)-1-((5R,6S)-6-methyl-7,8,9-trimethylene-3-oxa-tricyclo[3.2.2.0<sup>2,4</sup>]non-6-yl)-ethyl ester

82134-64-3

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Basic information

Product Name: 4-Bromo-benzoic acid (R)-1-((5R,6S)-6-methyl-7,8,9-trimethylene-3-oxa-tricyclo[3.2.2.0^2,4]non-6-yl)-ethyl ester
Synonyms: 4-Bromo-benzoic acid (R)-1-((5R,6S)-6-methyl-7,8,9-trimethylene-3-oxa-tricyclo[3.2.2.0^2,4]non-6-yl)-ethyl ester
CAS NO:82134-64-3
Molecular Formula:
Molecular Weight: 401.3
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: 4-Bromo-benzoic acid (R)-1-((5R,6S)-6-methyl-7,8,9-trimethylene-3-oxa-tricyclo[3.2.2.0^2,4]non-6-yl)-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-Bromo-benzoic acid (R)-1-((5R,6S)-6-methyl-7,8,9-trimethylene-3-oxa-tricyclo[3.2.2.0^2,4]non-6-yl)-ethyl ester(82134-64-3)
EPA Substance Registry System: 4-Bromo-benzoic acid (R)-1-((5R,6S)-6-methyl-7,8,9-trimethylene-3-oxa-tricyclo[3.2.2.0^2,4]non-6-yl)-ethyl ester(82134-64-3)

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: 82134-64-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 82134-64-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,3 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82134-64:
(7*8)+(6*2)+(5*1)+(4*3)+(3*4)+(2*6)+(1*4)=113
113 % 10 = 3
So 82134-64-3 is a valid CAS Registry Number.

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82134-64-3Relevant academic research and scientific papers

Chemo-, Regio-, and Stereoselective Hydroalumination of 7,8-Epoxy-2,3,5,6-tetramethylenebicyclooctane

Gabioud, Raphy,Chapuis, Gervais,Vogel, Pierre

, p. 3316 - 3319 (1982)

The oxirane ring of 7,8-epoxy-2,3,5,6-tetramethylenebicyclooctane (1) was not reduced by NaAlH2(OCH2CH2OCH3)2.Hydroalumination of the syn diene occured instead with the formation of a η1-allylaluminate 5, which yielded selectively 1,2- o

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