Cas 112601-86-2,Pentanenitrile, 4-[(trimethylsilyl)oxy]-2-(triphenylphosphoranylidene)-, (S)-

112601-86-2

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Basic information

Product Name: Pentanenitrile, 4-[(trimethylsilyl)oxy]-2-(triphenylphosphoranylidene)-, (S)-
Synonyms:
CAS NO:112601-86-2
Molecular Formula: C26H30NOPSi
Molecular Weight: 431.59
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: Pentanenitrile, 4-[(trimethylsilyl)oxy]-2-(triphenylphosphoranylidene)-, (S)-(CAS DataBase Reference)
NIST Chemistry Reference: Pentanenitrile, 4-[(trimethylsilyl)oxy]-2-(triphenylphosphoranylidene)-, (S)-(112601-86-2)
EPA Substance Registry System: Pentanenitrile, 4-[(trimethylsilyl)oxy]-2-(triphenylphosphoranylidene)-, (S)-(112601-86-2)

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: 112601-86-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112601-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,6,0 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 112601-86:
(8*1)+(7*1)+(6*2)+(5*6)+(4*0)+(3*1)+(2*8)+(1*6)=82
82 % 10 = 2
So 112601-86-2 is a valid CAS Registry Number.

112601-86-2Upstream product

75-77-4 chloro-trimethyl-silane

112601-86-2Downstream Products

112601-86-2Relevant academic research and scientific papers

SYNTHESE VON γ-HYDROXYNITRILEN, γ-BUTYROLACTONEN UND α-METHYLENO-γ-BUTYROLACTONEN AUS EPOXIDEN UND NATRIUM-

Bestmann, Hans Juergen,Schmidt, Martin

, p. 2111 - 2114 (1987)

The highly nucleophilic ylide-anion of sodium- attacks oxiranes by ring-opening.Depending on the work-up-conditions and the further reactions being employed, γ-hydroxynitriles, γ-butyrolactones or α-methyleno-γ-butyrolactones are obtained from the primary products thus formed.

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