Cas 110036-07-2,((E)-4-Phenyl-2-triisopropylsilanyl-buta-1,3-dienylidene)-triisopropylsilanyl-amine

110036-07-2

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Basic information

Product Name: ((E)-4-Phenyl-2-triisopropylsilanyl-buta-1,3-dienylidene)-triisopropylsilanyl-amine
Synonyms: ((E)-4-Phenyl-2-triisopropylsilanyl-buta-1,3-dienylidene)-triisopropylsilanyl-amine
CAS NO:110036-07-2
Molecular Formula:
Molecular Weight: 455.875
EINECS: N/A
Product Categories: N/A
Mol File: 110036-07-2.mol
Article Data: 1

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: ((E)-4-Phenyl-2-triisopropylsilanyl-buta-1,3-dienylidene)-triisopropylsilanyl-amine(CAS DataBase Reference)
NIST Chemistry Reference: ((E)-4-Phenyl-2-triisopropylsilanyl-buta-1,3-dienylidene)-triisopropylsilanyl-amine(110036-07-2)
EPA Substance Registry System: ((E)-4-Phenyl-2-triisopropylsilanyl-buta-1,3-dienylidene)-triisopropylsilanyl-amine(110036-07-2)

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: 110036-07-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 110036-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,0,3 and 6 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 110036-07:
(8*1)+(7*1)+(6*0)+(5*0)+(4*3)+(3*6)+(2*0)+(1*7)=52
52 % 10 = 2
So 110036-07-2 is a valid CAS Registry Number.

110036-07-2Upstream product

110036-07-2Downstream Products

110036-07-2Relevant articles and documents

A VERSATILE METHOD OF SYNTHESIS OF ANILINES AND CYCLOHEXENONES

Differding, Edmond,Vandevelde, Oscar,Roekens, Bertrand,Van, Tran Trieu,Ghosez, Leon

, p. 397 - 400 (2007/10/02)

Allylic cyanides are readily silylated by triisopropylsilyl chloride to give alkenyl ketenimines 1.The reaction of 1 with acetylenic dienophiles followed by desilylation leads to the formation of substituted anilines with complete regioselectivity.

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