Cas 1034596-22-9,5-{(3R,4S,1'R)-3-[1'-(tert-butyldimethylsilyloxy)ethyl]-2-oxo-azetidin-4-yl}-4,7-dimethylene-2-phenyl-3a,4,7,7a-tetrahydro-isoindole-1,3-dione

1034596-22-9

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Product Name: 5-{(3R,4S,1'R)-3-[1'-(tert-butyldimethylsilyloxy)ethyl]-2-oxo-azetidin-4-yl}-4,7-dimethylene-2-phenyl-3a,4,7,7a-tetrahydro-isoindole-1,3-dione
Synonyms: 5-{(3R,4S,1'R)-3-[1'-(tert-butyldimethylsilyloxy)ethyl]-2-oxo-azetidin-4-yl}-4,7-dimethylene-2-phenyl-3a,4,7,7a-tetrahydro-isoindole-1,3-dione
CAS NO:1034596-22-9
Molecular Formula:
Molecular Weight: 478.663
EINECS: N/A
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Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
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Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 5-{(3R,4S,1'R)-3-[1'-(tert-butyldimethylsilyloxy)ethyl]-2-oxo-azetidin-4-yl}-4,7-dimethylene-2-phenyl-3a,4,7,7a-tetrahydro-isoindole-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: 5-{(3R,4S,1'R)-3-[1'-(tert-butyldimethylsilyloxy)ethyl]-2-oxo-azetidin-4-yl}-4,7-dimethylene-2-phenyl-3a,4,7,7a-tetrahydro-isoindole-1,3-dione(1034596-22-9)
EPA Substance Registry System: 5-{(3R,4S,1'R)-3-[1'-(tert-butyldimethylsilyloxy)ethyl]-2-oxo-azetidin-4-yl}-4,7-dimethylene-2-phenyl-3a,4,7,7a-tetrahydro-isoindole-1,3-dione(1034596-22-9)

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Safety Statements: N/A
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HazardClass: N/A
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Hazardous Substances Data: 1034596-22-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1034596-22-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,4,5,9 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1034596-22:
(9*1)+(8*0)+(7*3)+(6*4)+(5*5)+(4*9)+(3*6)+(2*2)+(1*2)=139
139 % 10 = 9
So 1034596-22-9 is a valid CAS Registry Number.

1034596-22-9Upstream product

1034596-22-9Downstream Products

1034596-45-6 5-{(3R,4S,1'R)-3-[1'-(tert-butyldimethylsilyloxy)ethyl]-2-oxo-azetidin-4-yl}-4,7-dimethyl-2-phenylisoindole-1,3-dione

1034596-22-9Relevant academic research and scientific papers

Indium-mediated 1,2,4,5-hexatetraen-3-ylation of 4-acetoxy-2-azetidinones and their applications to the Diels-Alder reactions for the synthesis of 2-azetidinone derivatives

Yu, Heashim,Lee, Phil Ho

, p. 5183 - 5186 (2008/12/20)

(Chemical Equation Presented) 4-Acetoxy-2-azetidinones reacted with organoindium reagent generated in situ from indium and 1,6-dibromo-2,4-hexadiyne in the presence of LiCl in DMF to selectively produce 2-azetidinones possessing 1,2,4,5-hexatetraen-3-yl group on the C4-position. The Diels-Alder reactions of 4-(1,2,4,5-hexatetraen-3-yl)-2-azetidinones with a variety of dienophiles and subsequent aromatizations afforded valuable functional group-substituted 2-azetidinones in good yields.

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