Cas 123294-97-3,(R)-Acetoxy-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-acetic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

123294-97-3

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Basic information

Product Name: (R)-Acetoxy-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-acetic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester
Synonyms: (R)-Acetoxy-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-acetic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester
CAS NO:123294-97-3
Molecular Formula:
Molecular Weight: 466.574
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: (R)-Acetoxy-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-acetic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-Acetoxy-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-acetic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(123294-97-3)
EPA Substance Registry System: (R)-Acetoxy-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-acetic acid (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(123294-97-3)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 123294-97-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 123294-97-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,2,9 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 123294-97:
(8*1)+(7*2)+(6*3)+(5*2)+(4*9)+(3*4)+(2*9)+(1*7)=123
123 % 10 = 3
So 123294-97-3 is a valid CAS Registry Number.

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123294-97-3Relevant academic research and scientific papers

STEREOSELECTIVE ACETOXYLATION OF CHIRAL PHENYLACETIC ESTERS

Guy, Alain,Lemor, Alain,Imbert, Dominique,Lemaire, Marc

, p. 327 - 330 (1989)

Asymmetric oxidation of substituted phenylacetic acids was performed using D.D.Q. as oxidizing agent.The formation of a donor-acceptor intermediate complex between substrate and reagent accounted for the d.e. observed and the configuration of the major pr

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