Cas 210291-41-1,(2R,3R,6R)-2-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-6-isopropyl-3-methyl-cyclohexanone

210291-41-1

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Basic information

Product Name: (2R,3R,6R)-2-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-6-isopropyl-3-methyl-cyclohexanone
Synonyms: (2R,3R,6R)-2-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-6-isopropyl-3-methyl-cyclohexanone
CAS NO:210291-41-1
Molecular Formula:
Molecular Weight: 326.595
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,6R)-2-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-6-isopropyl-3-methyl-cyclohexanone(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,6R)-2-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-6-isopropyl-3-methyl-cyclohexanone(210291-41-1)
EPA Substance Registry System: (2R,3R,6R)-2-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-6-isopropyl-3-methyl-cyclohexanone(210291-41-1)

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: 210291-41-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 210291-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,2,9 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 210291-41:
(8*2)+(7*1)+(6*0)+(5*2)+(4*9)+(3*1)+(2*4)+(1*1)=81
81 % 10 = 1
So 210291-41-1 is a valid CAS Registry Number.

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210291-41-1Relevant academic research and scientific papers

Synthesis and proof of stereostructure of a new (+)-isomenthone-derived homochiral 1,3-diol

Gardiner, John M.,Chughtai, Jameel H.,Sadler, Ian H.

, p. 599 - 606 (1998)

Diastereopure (+)-isomenthone-derived ketoalcohol 2 was converted to the homochiral 1,3-diol 6 either by direct reduction or reduction of silyl protected derivatives. The diastereomeric preference of the reduction was the same in all cases. Reduction of 2

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