Cas 1320359-53-2,methyl 5-methylene-2-oxo-3-(2-(phenylsulfonyl)ethyl)tetrahydrofuran-3-carboxylate

1320359-53-2

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Basic information

Product Name: methyl 5-methylene-2-oxo-3-(2-(phenylsulfonyl)ethyl)tetrahydrofuran-3-carboxylate
Synonyms: methyl 5-methylene-2-oxo-3-(2-(phenylsulfonyl)ethyl)tetrahydrofuran-3-carboxylate
CAS NO:1320359-53-2
Molecular Formula:
Molecular Weight: 324.354
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: methyl 5-methylene-2-oxo-3-(2-(phenylsulfonyl)ethyl)tetrahydrofuran-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 5-methylene-2-oxo-3-(2-(phenylsulfonyl)ethyl)tetrahydrofuran-3-carboxylate(1320359-53-2)
EPA Substance Registry System: methyl 5-methylene-2-oxo-3-(2-(phenylsulfonyl)ethyl)tetrahydrofuran-3-carboxylate(1320359-53-2)

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: 1320359-53-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1320359-53-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,0,3,5 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1320359-53:
(9*1)+(8*3)+(7*2)+(6*0)+(5*3)+(4*5)+(3*9)+(2*5)+(1*3)=122
122 % 10 = 2
So 1320359-53-2 is a valid CAS Registry Number.

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1320359-53-2Relevant academic research and scientific papers

Tandem cyclization-Michael reaction by combination of metal- and organocatalysis

Aleman, Jose,Del Solar, Virginia,Martin-Santos, Cecilia,Cubo, Leticia,Ranninger, Carmen Navarro

, p. 7287 - 7293 (2011)

The use of a catalytic amount of platinum complexes (1 mol%) was found to be compatible with different organocatalysts (DABCO or the Jorgensen- Hayashi catalyst) that were used in the functionalization of various activated methylenes. By this method, a series of lactones with C-3 quaternary centers and substitution at C-5 were prepared.

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