Cas 308239-94-3,1-[(3aR,4R,6R,6aR)-2,2-Dimethyl-6-(tetrahydro-pyran-2-yloxymethyl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-3-prop-2-ynyl-1H-pyrimidine-2,4-dione

308239-94-3

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Basic information

Product Name: 1-[(3aR,4R,6R,6aR)-2,2-Dimethyl-6-(tetrahydro-pyran-2-yloxymethyl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-3-prop-2-ynyl-1H-pyrimidine-2,4-dione
Synonyms:
CAS NO:308239-94-3
Molecular Formula:
Molecular Weight: 406.436
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: 1-[(3aR,4R,6R,6aR)-2,2-Dimethyl-6-(tetrahydro-pyran-2-yloxymethyl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-3-prop-2-ynyl-1H-pyrimidine-2,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: 1-[(3aR,4R,6R,6aR)-2,2-Dimethyl-6-(tetrahydro-pyran-2-yloxymethyl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-3-prop-2-ynyl-1H-pyrimidine-2,4-dione(308239-94-3)
EPA Substance Registry System: 1-[(3aR,4R,6R,6aR)-2,2-Dimethyl-6-(tetrahydro-pyran-2-yloxymethyl)-tetrahydro-furo[3,4-d][1,3]dioxol-4-yl]-3-prop-2-ynyl-1H-pyrimidine-2,4-dione(308239-94-3)

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: 308239-94-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 308239-94-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,8,2,3 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 308239-94:
(8*3)+(7*0)+(6*8)+(5*2)+(4*3)+(3*9)+(2*9)+(1*4)=143
143 % 10 = 3
So 308239-94-3 is a valid CAS Registry Number.

308239-94-3Upstream product

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308239-94-3Relevant academic research and scientific papers

Palladium catalysed tandem cyclisation-anion capture. Part 6: Synthesis of sugar, nucleoside, purine, benzodiazepinone and β-lactam analogues via capture of in situ generated vinylstannanes

Casaschi, Adele,Grigg, Ronald,Sansano, José M.

, p. 7553 - 7560 (2000)

The regioselective palladium catalysed hydrostannylation of alkynes bearing a β-heteroatom affords mainly α-vinyltin(IV) compounds that are used as terminating species in palladium catalysed cyclisation-anion capture processes. The pharmacophore attached

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