Cas 131225-80-4,Benzoic acid (1R,2S,4R,5R,6S)-1-(3-oxa-tricyclo[3.2.1.0<sup>2,4</sup>]oct-6-yl)-ethyl ester

131225-80-4

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Basic information

Product Name: Benzoic acid (1R,2S,4R,5R,6S)-1-(3-oxa-tricyclo[3.2.1.0^2,4]oct-6-yl)-ethyl ester
Synonyms: Benzoic acid (1R,2S,4R,5R,6S)-1-(3-oxa-tricyclo[3.2.1.0^2,4]oct-6-yl)-ethyl ester
CAS NO:131225-80-4
Molecular Formula:
Molecular Weight: 258.317
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: Benzoic acid (1R,2S,4R,5R,6S)-1-(3-oxa-tricyclo[3.2.1.0^2,4]oct-6-yl)-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid (1R,2S,4R,5R,6S)-1-(3-oxa-tricyclo[3.2.1.0^2,4]oct-6-yl)-ethyl ester(131225-80-4)
EPA Substance Registry System: Benzoic acid (1R,2S,4R,5R,6S)-1-(3-oxa-tricyclo[3.2.1.0^2,4]oct-6-yl)-ethyl ester(131225-80-4)

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: 131225-80-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 131225-80-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,2,2 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 131225-80:
(8*1)+(7*3)+(6*1)+(5*2)+(4*2)+(3*5)+(2*8)+(1*0)=84
84 % 10 = 4
So 131225-80-4 is a valid CAS Registry Number.

131225-80-4Upstream product

131225-79-1 1-(bicyclo<2.2.1>hept-5-en-2-yl)ethyl benzoate

131225-80-4Downstream Products

131225-80-4Relevant academic research and scientific papers

Epoxidation of Olefins with Molecular Oxygen and Alcohol Catalyzed by Bis(2-alkyl-1,3-diketonato)oxovanadium(IV)

Takai, Toshihiro,Yamada, Tohru,Mukaiyama, Teruaki

, p. 1657 - 1660 (1990)

By combined use of molecular oxygen (oxidant) and secondary or primary alocohol (reductant) in the presence of a catalytic amount of bis(2-alkyl-1,3-diketonato)oxovanadium(IV) complexes, norbornene analogues are monooxygenated into the corresponding epoxides in good yields.

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