Cas 1028868-29-2,(<sup>Si</sup>S,R)-2-[2-(1-tert-butyl-1-silaindan-1-yloxy)-2-phenyl-4-(trimethylsilanyl)-but-3-ynyl]pyridine

1028868-29-2

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Basic information

Product Name: (^SiS,R)-2-[2-(1-tert-butyl-1-silaindan-1-yloxy)-2-phenyl-4-(trimethylsilanyl)-but-3-ynyl]pyridine
Synonyms:
CAS NO:1028868-29-2
Molecular Formula:
Molecular Weight: 483.801
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: (^SiS,R)-2-[2-(1-tert-butyl-1-silaindan-1-yloxy)-2-phenyl-4-(trimethylsilanyl)-but-3-ynyl]pyridine(CAS DataBase Reference)
NIST Chemistry Reference: (^SiS,R)-2-[2-(1-tert-butyl-1-silaindan-1-yloxy)-2-phenyl-4-(trimethylsilanyl)-but-3-ynyl]pyridine(1028868-29-2)
EPA Substance Registry System: (^SiS,R)-2-[2-(1-tert-butyl-1-silaindan-1-yloxy)-2-phenyl-4-(trimethylsilanyl)-but-3-ynyl]pyridine(1028868-29-2)

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: 1028868-29-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1028868-29-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,8,8,6 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1028868-29:
(9*1)+(8*0)+(7*2)+(6*8)+(5*8)+(4*6)+(3*8)+(2*2)+(1*9)=172
172 % 10 = 2
So 1028868-29-2 is a valid CAS Registry Number.

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1028868-29-2Relevant academic research and scientific papers

Kinetic resolution of donor-functionalised tertiary alcohols by Cu-H-catalysed stereoselective silylation using a strained silicon-stereogenic silane

Karatas, Betuel,Rendler, Sebastian,Froehlich, Roland,Oestreich, Martin

, p. 1435 - 1440 (2008)

A series of propargylic tertiary alcohols decorated with an sp 2-hybridised nitrogen donor were kinetically resolved by reagent-controlled dehydrogenative Si-O coupling with a strained, highly reactive silicon-stereogenic cyclic silane. The Royal Society of Chemistry.

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