Cas 1361325-63-4,(1R,5R,7R)-7-(4-chlorophenyl)-5-isopropyl-2-methyl-6-oxabicyclo[3.2.1]oct-2-ene

1361325-63-4

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Basic information

Product Name: (1R,5R,7R)-7-(4-chlorophenyl)-5-isopropyl-2-methyl-6-oxabicyclo[3.2.1]oct-2-ene
Synonyms: (1R,5R,7R)-7-(4-chlorophenyl)-5-isopropyl-2-methyl-6-oxabicyclo[3.2.1]oct-2-ene
CAS NO:1361325-63-4
Molecular Formula:
Molecular Weight: 276.806
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: (1R,5R,7R)-7-(4-chlorophenyl)-5-isopropyl-2-methyl-6-oxabicyclo[3.2.1]oct-2-ene(CAS DataBase Reference)
NIST Chemistry Reference: (1R,5R,7R)-7-(4-chlorophenyl)-5-isopropyl-2-methyl-6-oxabicyclo[3.2.1]oct-2-ene(1361325-63-4)
EPA Substance Registry System: (1R,5R,7R)-7-(4-chlorophenyl)-5-isopropyl-2-methyl-6-oxabicyclo[3.2.1]oct-2-ene(1361325-63-4)

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: 1361325-63-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1361325-63-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,1,3,2 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1361325-63:
(9*1)+(8*3)+(7*6)+(6*1)+(5*3)+(4*2)+(3*5)+(2*6)+(1*3)=134
134 % 10 = 4
So 1361325-63-4 is a valid CAS Registry Number.

1361325-63-4Upstream product

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1361325-63-4Relevant academic research and scientific papers

Stereoselective synthesis of 6-oxabicyclo[3.2.1]octene via (3,5)-oxonium-ene reaction

Saha, Pipas,Saikia, Anil K.

, p. 2261 - 2266 (2012)

Oxabicyclo[3.2.1]octene can efficiently be synthesized by the reaction of (-)-terpinen-4-ol and aldehyde or epoxide catalyzed by indium triflate (In(OTf)3) in good yields. The reaction is stereoselective and proceeds via (3,5)-oxonium-ene-type

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