Cas 104898-13-7,(2R,3R)-2,3-Dimethyl-succinic acid methyl ester (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester

104898-13-7

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Basic information

Product Name: (2R,3R)-2,3-Dimethyl-succinic acid methyl ester (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester
Synonyms:
CAS NO:104898-13-7
Molecular Formula:
Molecular Weight: 374.521
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: (2R,3R)-2,3-Dimethyl-succinic acid methyl ester (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R)-2,3-Dimethyl-succinic acid methyl ester (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(104898-13-7)
EPA Substance Registry System: (2R,3R)-2,3-Dimethyl-succinic acid methyl ester (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenyl-ethyl)-cyclohexyl ester(104898-13-7)

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: 104898-13-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 104898-13-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,9 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104898-13:
(8*1)+(7*0)+(6*4)+(5*8)+(4*9)+(3*8)+(2*1)+(1*3)=137
137 % 10 = 7
So 104898-13-7 is a valid CAS Registry Number.

104898-13-7Upstream product

186581-53-3 diazomethane

104898-13-7Downstream Products

104898-13-7Relevant academic research and scientific papers

ENANTIOSELECTIVE MICHAEL REACTIONS. STEREOSELECTIVE ADDITION OF ENOLATES OF PHENMENTHOL ESTERS TO CROTONATES.

Corey, E. J.,Peterson, Richard T.

, p. 5025 - 5028 (1985)

A method is described for enantioselective synthesis which is based on the stereoselective Michael addition of phenmenthol enolates such as 5 to E-crotonate esters.A stereomechanistic rationale is presented.

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