Cas 108945-24-0,(2S,3S)-3-Hydroxy-2-methyl-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester

108945-24-0

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Basic information

Product Name: (2S,3S)-3-Hydroxy-2-methyl-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester
Synonyms: (2S,3S)-3-Hydroxy-2-methyl-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester
CAS NO:108945-24-0
Molecular Formula:
Molecular Weight: 256.386
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: (2S,3S)-3-Hydroxy-2-methyl-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S)-3-Hydroxy-2-methyl-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(108945-24-0)
EPA Substance Registry System: (2S,3S)-3-Hydroxy-2-methyl-butyric acid (1R,2S,5R)-2-isopropyl-5-methyl-cyclohexyl ester(108945-24-0)

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: 108945-24-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 108945-24-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,9,4 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108945-24:
(8*1)+(7*0)+(6*8)+(5*9)+(4*4)+(3*5)+(2*2)+(1*4)=140
140 % 10 = 0
So 108945-24-0 is a valid CAS Registry Number.

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108945-24-0Relevant academic research and scientific papers

FACTORS AFFECTING STEREOCHEMICAL CONTROL IN DIRECTED HOMOGENEOUS HYDROGENATION OF α-HYDROXYALKYLARCYLATES

Brown, John M.,Cutting, Ian,Evans, Phillip L.,Maddox, Peter J.

, p. 3307 - 3310 (2007/10/02)

The degree of asymmetric induction observed in hydrogenation of menthyl 3-hydroxy-2-methylenebutyrates catalysed by DIPAMP-Rh+ complexes is strongly dependent on anti-reduction product is formed with high enantioselection.

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