Cas 124502-82-5,2-[((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-hydroxy-methyl]-dihydro-pyran-3-one

124502-82-5

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Basic information

Product Name: 2-[((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-hydroxy-methyl]-dihydro-pyran-3-one
Synonyms: 2-[((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-hydroxy-methyl]-dihydro-pyran-3-one
CAS NO:124502-82-5
Molecular Formula:
Molecular Weight: 378.422
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: 2-[((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-hydroxy-methyl]-dihydro-pyran-3-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-[((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-hydroxy-methyl]-dihydro-pyran-3-one(124502-82-5)
EPA Substance Registry System: 2-[((3aR,5R,6S,6aR)-6-Benzyloxy-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-hydroxy-methyl]-dihydro-pyran-3-one(124502-82-5)

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: 124502-82-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 124502-82-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,5,0 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 124502-82:
(8*1)+(7*2)+(6*4)+(5*5)+(4*0)+(3*2)+(2*8)+(1*2)=95
95 % 10 = 5
So 124502-82-5 is a valid CAS Registry Number.

124502-82-5Upstream product

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124502-82-5Relevant academic research and scientific papers

REGIOSPECIFIC TETRAHYDROPYRAN-3-ONE ENOLATES. SYNTHESIS AND REACTIVITY OF SILYL ENOL ETHER DERIVATIVES

Cox, Paul,Mahon, Mary F,Molloy, Kieran C,Lister, Simon,Gallagher, Timothy

, p. 2437 - 2440 (2007/10/02)

The synthesis and reactivity of silyl enol ether (3) is reported.This reagent complements the reactivity of the lithiated enol ether (2) previously used as a synthetic equivalent of the regiospecific tetrahydropyran-3-one enolate (1).

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