Cas 115993-96-9,(1,2,3-Tri-tert-butyl-cycloprop-2-enyl)-[1-(2,4,6-trimethyl-phenyl)-1-trimethylsilanyloxy-meth-(Z)-ylidene]-phosphane

115993-96-9

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Basic information

Product Name: (1,2,3-Tri-tert-butyl-cycloprop-2-enyl)-[1-(2,4,6-trimethyl-phenyl)-1-trimethylsilanyloxy-meth-(Z)-ylidene]-phosphane
Synonyms:
CAS NO:115993-96-9
Molecular Formula:
Molecular Weight: 458.74
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: (1,2,3-Tri-tert-butyl-cycloprop-2-enyl)-[1-(2,4,6-trimethyl-phenyl)-1-trimethylsilanyloxy-meth-(Z)-ylidene]-phosphane(CAS DataBase Reference)
NIST Chemistry Reference: (1,2,3-Tri-tert-butyl-cycloprop-2-enyl)-[1-(2,4,6-trimethyl-phenyl)-1-trimethylsilanyloxy-meth-(Z)-ylidene]-phosphane(115993-96-9)
EPA Substance Registry System: (1,2,3-Tri-tert-butyl-cycloprop-2-enyl)-[1-(2,4,6-trimethyl-phenyl)-1-trimethylsilanyloxy-meth-(Z)-ylidene]-phosphane(115993-96-9)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 115993-96-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 115993-96-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,9,9 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 115993-96:
(8*1)+(7*1)+(6*5)+(5*9)+(4*9)+(3*3)+(2*9)+(1*6)=159
159 % 10 = 9
So 115993-96-9 is a valid CAS Registry Number.

115993-96-9Upstream product

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115993-96-9Relevant academic research and scientific papers

Phosphorverbindungen ungewoehnlicher Koordination. XXV. Cyclopropenyl-phosphaalkene, Edukte zur Synthese stabiler 2H-Phosphole

Zurmuehlen, Frank,Regitz, Manfred

, p. C1 - C5 (2007/10/02)

Reaction of a cyclopropenylium salt with lithium bis(trimethylsilyl)phosphide*2THF yields a phosphinocyclopropene.Replacement of a trimethylsilyl group by lithium followed by acylation with acid chlorides and relocation of silyl group leads to cyclopropen

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