Cas 85696-03-3,(1S,2S,4S)-Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid (1R,2S,3R,4S)-3-benzhydryloxy-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester

85696-03-3

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Basic information

Product Name: (1S,2S,4S)-Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid (1R,2S,3R,4S)-3-benzhydryloxy-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester
Synonyms:
CAS NO:85696-03-3
Molecular Formula:
Molecular Weight: 456.625
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,2S,4S)-Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid (1R,2S,3R,4S)-3-benzhydryloxy-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S,4S)-Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid (1R,2S,3R,4S)-3-benzhydryloxy-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester(85696-03-3)
EPA Substance Registry System: (1S,2S,4S)-Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid (1R,2S,3R,4S)-3-benzhydryloxy-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester(85696-03-3)

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: 85696-03-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 85696-03-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,9 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85696-03:
(7*8)+(6*5)+(5*6)+(4*9)+(3*6)+(2*0)+(1*3)=173
173 % 10 = 3
So 85696-03-3 is a valid CAS Registry Number.

85696-03-3Upstream product

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85696-03-3Relevant academic research and scientific papers

HIGH ASYMMETRIC INDUCTION IN DIELS-ALDER ADDITIONS OF CYCLOPENTADIENE TO ACRYLATES DERIVED FROM ISOBORNEOL

Oppolzer, Wolfgang,Chapuis, Christian,Dao, Guo Mao,Reichlin, Daniel,Godel, Thierry

, p. 4781 - 4784 (1982)

Starting from (R)-(+)- and from (S)-(-)-camphor the chiral alcohols 1, 2 and 3 have been prepared; their acrylates II underwent TiCl2(OR)2-promoted Diels-Alder additions to cyclopentadiene giving efficiently in a predictable manner either the (2R)- or the (2S)-adducts III with up to virtually quantitative asymmetric induction.

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