Cas 80781-00-6,methyl 2-t-butyldimethylsilyloxymethyl-3-trimethylsilyloxy-3-vinyl-Δ<sup>1,α</sup>-cyclobutaneacetate

80781-00-6

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Basic information

Product Name: methyl 2-t-butyldimethylsilyloxymethyl-3-trimethylsilyloxy-3-vinyl-Δ^1,α-cyclobutaneacetate
Synonyms:
CAS NO:80781-00-6
Molecular Formula:
Molecular Weight: 384.663
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 2-t-butyldimethylsilyloxymethyl-3-trimethylsilyloxy-3-vinyl-Δ^1,α-cyclobutaneacetate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2-t-butyldimethylsilyloxymethyl-3-trimethylsilyloxy-3-vinyl-Δ^1,α-cyclobutaneacetate(80781-00-6)
EPA Substance Registry System: methyl 2-t-butyldimethylsilyloxymethyl-3-trimethylsilyloxy-3-vinyl-Δ^1,α-cyclobutaneacetate(80781-00-6)

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: 80781-00-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 80781-00-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,8 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80781-00:
(7*8)+(6*0)+(5*7)+(4*8)+(3*1)+(2*0)+(1*0)=126
126 % 10 = 6
So 80781-00-6 is a valid CAS Registry Number.

80781-00-6Upstream product

80781-00-6Downstream Products

80780-99-0 methyl 2-(2-t-butyldimethylsilyloxyethylidene)-4-hydroxy-1-cyclohexanecarboxylate

80781-00-6Relevant academic research and scientific papers

Regiospecific Synthesis of Bicyclic 6-Alkoxy-2-pyrones and Their Use in the Production of Tetracyclic Intermediates for 11-Deoxyanthracycline Synthesis

Jung, Michael E.,Node, Manabu,Pfluger, Rudolf W.,Lyster, Mark A.,Lowe, John A.

, p. 1150 - 1152 (1982)

A regiospecific approach to the preparation of bicyclic 6-alkoxy-2-pyrones and their utilization in anthracycline synthesis is described.

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