Cas 88080-32-4,(S)-3,3,4,4-Tetramethyl-2-phenyl-oxetane-2-carboxylic acid (1S,2R,3S,4R)-3-(2,2-dimethyl-propoxy)-4,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester

88080-32-4

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Basic information

Product Name: (S)-3,3,4,4-Tetramethyl-2-phenyl-oxetane-2-carboxylic acid (1S,2R,3S,4R)-3-(2,2-dimethyl-propoxy)-4,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester
Synonyms:
CAS NO:88080-32-4
Molecular Formula:
Molecular Weight: 456.666
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: (S)-3,3,4,4-Tetramethyl-2-phenyl-oxetane-2-carboxylic acid (1S,2R,3S,4R)-3-(2,2-dimethyl-propoxy)-4,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3,3,4,4-Tetramethyl-2-phenyl-oxetane-2-carboxylic acid (1S,2R,3S,4R)-3-(2,2-dimethyl-propoxy)-4,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester(88080-32-4)
EPA Substance Registry System: (S)-3,3,4,4-Tetramethyl-2-phenyl-oxetane-2-carboxylic acid (1S,2R,3S,4R)-3-(2,2-dimethyl-propoxy)-4,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester(88080-32-4)

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: 88080-32-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 88080-32-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,8 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 88080-32:
(7*8)+(6*8)+(5*0)+(4*8)+(3*0)+(2*3)+(1*2)=144
144 % 10 = 4
So 88080-32-4 is a valid CAS Registry Number.

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88080-32-4Relevant academic research and scientific papers

INVESTIGATION OF CHIRAL INDUCTION IN PHOTOCHEMICAL OXETANE FORMATION

Koch, H.,Runsink, J.,Scharf, H.-D.

, p. 3217 - 3220 (1983)

The formation of oxetanes from photochemical addition of tetramethylethylene (TME) or diethylketeneacetal with phenylglyoxylic acid esters in the "concave" position leads to high diastereomeric excess (de).

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