Cas 819867-60-2,1-[[(E)-4-(tert-butyldimethylsilyloxy)but-2-enyl]-(4-methylbenzenesulfonyl)amino]-3-trimethylsilylprop-2-yne

819867-60-2

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Basic information

Product Name: 1-[[(E)-4-(tert-butyldimethylsilyloxy)but-2-enyl]-(4-methylbenzenesulfonyl)amino]-3-trimethylsilylprop-2-yne
Synonyms: 1-[[(E)-4-(tert-butyldimethylsilyloxy)but-2-enyl]-(4-methylbenzenesulfonyl)amino]-3-trimethylsilylprop-2-yne
CAS NO:819867-60-2
Molecular Formula:
Molecular Weight: 465.805
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-[[(E)-4-(tert-butyldimethylsilyloxy)but-2-enyl]-(4-methylbenzenesulfonyl)amino]-3-trimethylsilylprop-2-yne(CAS DataBase Reference)
NIST Chemistry Reference: 1-[[(E)-4-(tert-butyldimethylsilyloxy)but-2-enyl]-(4-methylbenzenesulfonyl)amino]-3-trimethylsilylprop-2-yne(819867-60-2)
EPA Substance Registry System: 1-[[(E)-4-(tert-butyldimethylsilyloxy)but-2-enyl]-(4-methylbenzenesulfonyl)amino]-3-trimethylsilylprop-2-yne(819867-60-2)

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: 819867-60-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 819867-60-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,9,8,6 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 819867-60:
(8*8)+(7*1)+(6*9)+(5*8)+(4*6)+(3*7)+(2*6)+(1*0)=222
222 % 10 = 2
So 819867-60-2 is a valid CAS Registry Number.

819867-60-2Upstream product

819867-60-2Downstream Products

819867-60-2Relevant academic research and scientific papers

Ruthenium-catalyzed enyne cycloisomerizations. Effect of allylic silyl ether on regioselectivity

Trost, Barry M.,Surivet, Jean-Philippe,Toste, F. Dean

, p. 15592 - 15602 (2007/10/03)

The ruthenium-catalyzed cycloisomerization of 1,6- and 1,7-enynes substituted in the terminal allylic position with a tert-butyldimethylsilyl ether group emerges as an effective reaction to form unprecedented five- or six-membered rings possessing a geome

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