Cas 1196033-48-3,(4R,2E)-4-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-yl)-4-(2-methoxyphenyl)but-2-enyl ethyl carbonate

1196033-48-3

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Basic information

Product Name: (4R,2E)-4-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-yl)-4-(2-methoxyphenyl)but-2-enyl ethyl carbonate
Synonyms:
CAS NO:1196033-48-3
Molecular Formula:
Molecular Weight: 392.406
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: (4R,2E)-4-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-yl)-4-(2-methoxyphenyl)but-2-enyl ethyl carbonate(CAS DataBase Reference)
NIST Chemistry Reference: (4R,2E)-4-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-yl)-4-(2-methoxyphenyl)but-2-enyl ethyl carbonate(1196033-48-3)
EPA Substance Registry System: (4R,2E)-4-(2,2-dimethyl-4,6-dioxo-1,3-dioxan-5-yl)-4-(2-methoxyphenyl)but-2-enyl ethyl carbonate(1196033-48-3)

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: 1196033-48-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1196033-48-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,6,0,3 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1196033-48:
(9*1)+(8*1)+(7*9)+(6*6)+(5*0)+(4*3)+(3*3)+(2*4)+(1*8)=153
153 % 10 = 3
So 1196033-48-3 is a valid CAS Registry Number.

1196033-48-3Upstream product

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1196033-48-3Relevant academic research and scientific papers

Asymmetrie addition of alkenylstannanes to alkylidene meldrum's acids

Mahoney, Stuart J.,Dumas, Aaron M.,Fillion, Eric

supporting information; experimental part, p. 5346 - 5349 (2010/02/28)

Herein, we describe enantioselective addition of alkenyltin reagents possessing a reactive and sensitive allylic functionality not readily available to other classes of alkenyl metals. This method is enabled by the use of highly electrophilic alkylidene M

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