Cas 160701-54-2,1-{5-(tert-Butyl-dimethyl-silanyloxy)-2-[2-(tert-butyl-dimethyl-silanyloxy)-3-propylamino-propoxy]-phenyl}-3-phenyl-propan-1-one

160701-54-2

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Basic information

Product Name: 1-{5-(tert-Butyl-dimethyl-silanyloxy)-2-[2-(tert-butyl-dimethyl-silanyloxy)-3-propylamino-propoxy]-phenyl}-3-phenyl-propan-1-one
Synonyms: 1-{5-(tert-Butyl-dimethyl-silanyloxy)-2-[2-(tert-butyl-dimethyl-silanyloxy)-3-propylamino-propoxy]-phenyl}-3-phenyl-propan-1-one
CAS NO:160701-54-2
Molecular Formula:
Molecular Weight: 585.975
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: 1-{5-(tert-Butyl-dimethyl-silanyloxy)-2-[2-(tert-butyl-dimethyl-silanyloxy)-3-propylamino-propoxy]-phenyl}-3-phenyl-propan-1-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-{5-(tert-Butyl-dimethyl-silanyloxy)-2-[2-(tert-butyl-dimethyl-silanyloxy)-3-propylamino-propoxy]-phenyl}-3-phenyl-propan-1-one(160701-54-2)
EPA Substance Registry System: 1-{5-(tert-Butyl-dimethyl-silanyloxy)-2-[2-(tert-butyl-dimethyl-silanyloxy)-3-propylamino-propoxy]-phenyl}-3-phenyl-propan-1-one(160701-54-2)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 160701-54-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 160701-54-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,7,0 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 160701-54:
(8*1)+(7*6)+(6*0)+(5*7)+(4*0)+(3*1)+(2*5)+(1*4)=102
102 % 10 = 2
So 160701-54-2 is a valid CAS Registry Number.

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160701-54-2Relevant academic research and scientific papers

Selective removal of phenolic and alcoholic silyl ethers

Prakash, Chandra,Saleh, Samir,Blair, Lan A.

, p. 7565 - 7568 (1994)

Potassium carbonate/Kriptofix 222 and pyridinium p-toluenesulfonate or BF3-etherate have been found to remove the tert-butyldimethylsilyl group from phenolic and alcoholic silyl ethers, respectively. This methodology should find wide applicability in complex organic synthesis.

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