Cas 104461-88-3,4,4-Dimethyl-2-oxo-cyclopentanecarboxylic acid (1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester

104461-88-3

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Basic information

Product Name: 4,4-Dimethyl-2-oxo-cyclopentanecarboxylic acid (1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester
Synonyms:
CAS NO:104461-88-3
Molecular Formula:
Molecular Weight: 294.434
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: 4,4-Dimethyl-2-oxo-cyclopentanecarboxylic acid (1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4,4-Dimethyl-2-oxo-cyclopentanecarboxylic acid (1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester(104461-88-3)
EPA Substance Registry System: 4,4-Dimethyl-2-oxo-cyclopentanecarboxylic acid (1S,2R,5S)-2-isopropyl-5-methyl-cyclohexyl ester(104461-88-3)

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: 104461-88-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 104461-88-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,4,6 and 1 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 104461-88:
(8*1)+(7*0)+(6*4)+(5*4)+(4*6)+(3*1)+(2*8)+(1*8)=103
103 % 10 = 3
So 104461-88-3 is a valid CAS Registry Number.

104461-88-3Upstream product

104461-88-3Downstream Products

104461-75-8 1,4,4-Trimethyl-2-oxo-cyclopentanecarboxylic acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

104461-88-3Relevant academic research and scientific papers

BOTRYDIAL SYNTHETIC STUDIES. ASYMMETRIC SYNTHESIS OF QUATERNARY CARBON CENTRES.

Kunisch, Franz,Hobert, Kurt,Welzel, Peter

, p. 5433 - 5436 (1985)

The synthesis of the optically active 4 has been accomplished by asymmetric formation of cyclic β-keto esters fully substituted at the α Carbon followed by chemoselective reduction of the ester group.Of the asymmetric reactions examined the Koga procedure proved to be the most selective.

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