Cas 1439461-59-2,(5E)-N-(8-(tert-butyldimethylsilyloxy)-8,8-dicyano-2-methyloct-5-en-4-yl)-4-methylbenzenesulfonamide

1439461-59-2

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Basic information

Product Name: (5E)-N-(8-(tert-butyldimethylsilyloxy)-8,8-dicyano-2-methyloct-5-en-4-yl)-4-methylbenzenesulfonamide
Synonyms: (5E)-N-(8-(tert-butyldimethylsilyloxy)-8,8-dicyano-2-methyloct-5-en-4-yl)-4-methylbenzenesulfonamide
CAS NO:1439461-59-2
Molecular Formula:
Molecular Weight: 475.728
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: (5E)-N-(8-(tert-butyldimethylsilyloxy)-8,8-dicyano-2-methyloct-5-en-4-yl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: (5E)-N-(8-(tert-butyldimethylsilyloxy)-8,8-dicyano-2-methyloct-5-en-4-yl)-4-methylbenzenesulfonamide(1439461-59-2)
EPA Substance Registry System: (5E)-N-(8-(tert-butyldimethylsilyloxy)-8,8-dicyano-2-methyloct-5-en-4-yl)-4-methylbenzenesulfonamide(1439461-59-2)

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: 1439461-59-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1439461-59-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,9,4,6 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1439461-59:
(9*1)+(8*4)+(7*3)+(6*9)+(5*4)+(4*6)+(3*1)+(2*5)+(1*9)=182
182 % 10 = 2
So 1439461-59-2 is a valid CAS Registry Number.

1439461-59-2Upstream product

128302-78-3 α-(tert-butyldimethylsilyloxy)malonitrile

1439461-59-2Downstream Products

1439461-59-2Relevant academic research and scientific papers

Palladium-catalyzed highly regio- and stereoselective carbon-carbon bond formation reaction of γ-substituted vinylaziridines with a silylated masked acyl cyanide reagent

Kawamura, Tomoyuki,Matsuo, Nanae,Yamauchi, Daisuke,Tanabe, Yoo,Nemoto, Hisao

, p. 5331 - 5341 (2013/06/27)

Highly regio- and stereoselective carbon-carbon bond formation reaction of vinylaziridines using a masked acyl cyanide reagent possessing a tert-butyldimethylsilyl group occurred in the presence of a catalytic amount of palladium complex in excellent yield. It is considered that these excellent selectivities are the result of three simultaneous conditions, strained leaving group, small nucleophile, and ligand with small cone-angle.

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