Cas 1147845-96-2,(E)-1-[2-benzylidene-4-(tert-butyldimethylsilyl)-3-butynyl]piperidine

1147845-96-2

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Basic information

Product Name: (E)-1-[2-benzylidene-4-(tert-butyldimethylsilyl)-3-butynyl]piperidine
Synonyms: (E)-1-[2-benzylidene-4-(tert-butyldimethylsilyl)-3-butynyl]piperidine
CAS NO:1147845-96-2
Molecular Formula:
Molecular Weight: 339.596
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: (E)-1-[2-benzylidene-4-(tert-butyldimethylsilyl)-3-butynyl]piperidine(CAS DataBase Reference)
NIST Chemistry Reference: (E)-1-[2-benzylidene-4-(tert-butyldimethylsilyl)-3-butynyl]piperidine(1147845-96-2)
EPA Substance Registry System: (E)-1-[2-benzylidene-4-(tert-butyldimethylsilyl)-3-butynyl]piperidine(1147845-96-2)

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: 1147845-96-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1147845-96-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,7,8,4 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1147845-96:
(9*1)+(8*1)+(7*4)+(6*7)+(5*8)+(4*4)+(3*5)+(2*9)+(1*6)=182
182 % 10 = 2
So 1147845-96-2 is a valid CAS Registry Number.

1147845-96-2Upstream product

1147845-96-2Downstream Products

1147845-96-2Relevant academic research and scientific papers

Nickel- and rhodium-catalyzed addition of terminal silylacetylenes to propargyl amines: Catalyst-dependent complementary regioselectivity

Matsuyama, Naoto,Hirano, Koji,Satoh, Tetsuya,Miura, Masahiro

experimental part, p. 3576 - 3578 (2009/09/05)

The cross-addition of terminal silylacetylenes to γ-arylated propargyl amines occurs efficiently via C - H cleavage by using either a nickel or rhodium catalyst. Taking advantage of the catalyst-controlled switching of regioselectivity in the reaction, bo

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