Cas 210291-44-4,(1S,2S,3R,6R)-2-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-6-isopropyl-3-methyl-cyclohexanol

210291-44-4

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Basic information

Product Name: (1S,2S,3R,6R)-2-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-6-isopropyl-3-methyl-cyclohexanol
Synonyms: (1S,2S,3R,6R)-2-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-6-isopropyl-3-methyl-cyclohexanol
CAS NO:210291-44-4
Molecular Formula:
Molecular Weight: 328.611
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: (1S,2S,3R,6R)-2-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-6-isopropyl-3-methyl-cyclohexanol(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S,3R,6R)-2-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-6-isopropyl-3-methyl-cyclohexanol(210291-44-4)
EPA Substance Registry System: (1S,2S,3R,6R)-2-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-propyl]-6-isopropyl-3-methyl-cyclohexanol(210291-44-4)

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: 210291-44-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 210291-44-4 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 4 respectively.
Calculate Digit Verification of CAS Registry Number 210291-44:
(8*2)+(7*1)+(6*0)+(5*2)+(4*9)+(3*1)+(2*4)+(1*4)=84
84 % 10 = 4
So 210291-44-4 is a valid CAS Registry Number.

210291-44-4Upstream product

210291-44-4Downstream Products

210291-39-7 (1'R,1S,2R,3R,6R)-2-(1'-hydroxypropyl)-6-isopropyl-3-methylcyclohexanol

210291-44-4Relevant 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 (2007/10/03)

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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