Cas 1214890-93-3,methyl 6-((4-methoxybenzoyloxy)-methyl)-6-methyl-4-(methylsulfanyl)-2-oxo-5,6-dihydro-2H-pyran-3-carboxylate

1214890-93-3

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Basic information

Product Name: methyl 6-((4-methoxybenzoyloxy)-methyl)-6-methyl-4-(methylsulfanyl)-2-oxo-5,6-dihydro-2H-pyran-3-carboxylate
Synonyms: methyl 6-((4-methoxybenzoyloxy)-methyl)-6-methyl-4-(methylsulfanyl)-2-oxo-5,6-dihydro-2H-pyran-3-carboxylate
CAS NO:1214890-93-3
Molecular Formula:
Molecular Weight: 380.419
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 6-((4-methoxybenzoyloxy)-methyl)-6-methyl-4-(methylsulfanyl)-2-oxo-5,6-dihydro-2H-pyran-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 6-((4-methoxybenzoyloxy)-methyl)-6-methyl-4-(methylsulfanyl)-2-oxo-5,6-dihydro-2H-pyran-3-carboxylate(1214890-93-3)
EPA Substance Registry System: methyl 6-((4-methoxybenzoyloxy)-methyl)-6-methyl-4-(methylsulfanyl)-2-oxo-5,6-dihydro-2H-pyran-3-carboxylate(1214890-93-3)

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: 1214890-93-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1214890-93-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,4,8,9 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1214890-93:
(9*1)+(8*2)+(7*1)+(6*4)+(5*8)+(4*9)+(3*0)+(2*9)+(1*3)=153
153 % 10 = 3
So 1214890-93-3 is a valid CAS Registry Number.

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1214890-93-3Relevant academic research and scientific papers

Unprecedented 'ring transformation-rearrangement' of pyran-2-ones into 5,6-dihydropyran-2-ones through insertion of acetol

Kumar, Amit,Singh, Salil P.,Verma, Deepti,Kant, Ruchir,Maulik, Prakas R.,Goel, Atul

experimental part, p. 961 - 965 (2010/04/29)

One-pot efficient synthesis of functionalized 5,6-dihydropyran-2-ones has been delineated by reacting 2H-pyran-2-ones and acetol in the presence of a base at room temperature. The formation of 5,6-dihydropyran-2-ones revealed that the reaction proceeded in a unique 'ring transformation-rearrangement' sequence.

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