Cas 908261-07-4,4,7,7-trimethyl-3-oxo-2-oxa-bicyclo[2.2.1]heptane-1-carboxylic acid 2,3,3-trimethyl-1-phenyl-butyl ester

908261-07-4

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Basic information

Product Name: 4,7,7-trimethyl-3-oxo-2-oxa-bicyclo[2.2.1]heptane-1-carboxylic acid 2,3,3-trimethyl-1-phenyl-butyl ester
Synonyms: 4,7,7-trimethyl-3-oxo-2-oxa-bicyclo[2.2.1]heptane-1-carboxylic acid 2,3,3-trimethyl-1-phenyl-butyl ester
CAS NO:908261-07-4
Molecular Formula:
Molecular Weight: 372.505
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: 4,7,7-trimethyl-3-oxo-2-oxa-bicyclo[2.2.1]heptane-1-carboxylic acid 2,3,3-trimethyl-1-phenyl-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4,7,7-trimethyl-3-oxo-2-oxa-bicyclo[2.2.1]heptane-1-carboxylic acid 2,3,3-trimethyl-1-phenyl-butyl ester(908261-07-4)
EPA Substance Registry System: 4,7,7-trimethyl-3-oxo-2-oxa-bicyclo[2.2.1]heptane-1-carboxylic acid 2,3,3-trimethyl-1-phenyl-butyl ester(908261-07-4)

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: 908261-07-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 908261-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,2,6 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 908261-07:
(8*9)+(7*0)+(6*8)+(5*2)+(4*6)+(3*1)+(2*0)+(1*7)=164
164 % 10 = 4
So 908261-07-4 is a valid CAS Registry Number.

908261-07-4Upstream product

908261-07-4Downstream Products

908261-08-5 (-)-syn-2,3,3-trimethyl-1-phenyl-butan-1-ol

908261-07-4Relevant academic research and scientific papers

Chiral α-branched benzylic carbocations: Diastereoselective intermolecular reactions with arene nucleophiles and NMR spectroscopic studies

Muehlthau, Friedrich,Stadler, Daniel,Goeppert, Alain,Olah, George A.,Prakash, G. K. Surya,Bach, Thorsten

, p. 9668 - 9675 (2006)

The chiral benzylic alcohols 1-6 were prepared and subjected to S N1-type displacement reactions with various arene nucleophiles in acidic medium. Under optimized conditions (HBF4·OEt 2, CH2Cl2, -78 °

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