Cas 1167535-48-9,(1S,3R,5R)-5-{[tert-butyl(dimethyl)silyl]oxy}-1-cyclohexyl-7-phenylheptane-1,3-diol

1167535-48-9

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Basic information

Product Name: (1S,3R,5R)-5-{[tert-butyl(dimethyl)silyl]oxy}-1-cyclohexyl-7-phenylheptane-1,3-diol
Synonyms: (1S,3R,5R)-5-{[tert-butyl(dimethyl)silyl]oxy}-1-cyclohexyl-7-phenylheptane-1,3-diol
CAS NO:1167535-48-9
Molecular Formula:
Molecular Weight: 420.708
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,3R,5R)-5-{[tert-butyl(dimethyl)silyl]oxy}-1-cyclohexyl-7-phenylheptane-1,3-diol(CAS DataBase Reference)
NIST Chemistry Reference: (1S,3R,5R)-5-{[tert-butyl(dimethyl)silyl]oxy}-1-cyclohexyl-7-phenylheptane-1,3-diol(1167535-48-9)
EPA Substance Registry System: (1S,3R,5R)-5-{[tert-butyl(dimethyl)silyl]oxy}-1-cyclohexyl-7-phenylheptane-1,3-diol(1167535-48-9)

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: 1167535-48-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1167535-48-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,7,5,3 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1167535-48:
(9*1)+(8*1)+(7*6)+(6*7)+(5*5)+(4*3)+(3*5)+(2*4)+(1*8)=169
169 % 10 = 9
So 1167535-48-9 is a valid CAS Registry Number.

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1167535-48-9Relevant academic research and scientific papers

Stereoselective synthesis of syn,syn and syn,anti-1,3,5-triols via intramolecular hydrosilylation of substituted pent-3-en-1,5-diols

Li, Fangzheng,Roush, William R.

, p. 2932 - 2935 (2009)

A stereoselective method for synthesis of syn,syn- and syn,anti-1,3,5- trlols based on a double allylboration-Intramolecular hydrosllylation sequence has been developed. The 1,3-syn stereocontrol is achieved in the Intramolecular hydrosllylation of monopr

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