Cas 80900-60-3,2-(tert-Butyl-dimethyl-silanyloxy)-6-methoxy-1-(3-oxo-butyl)-cyclohexa-2,5-dienecarboxylic acid methyl ester

80900-60-3

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Basic information

Product Name: 2-(tert-Butyl-dimethyl-silanyloxy)-6-methoxy-1-(3-oxo-butyl)-cyclohexa-2,5-dienecarboxylic acid methyl ester
Synonyms:
CAS NO:80900-60-3
Molecular Formula:
Molecular Weight: 368.546
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-(tert-Butyl-dimethyl-silanyloxy)-6-methoxy-1-(3-oxo-butyl)-cyclohexa-2,5-dienecarboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-(tert-Butyl-dimethyl-silanyloxy)-6-methoxy-1-(3-oxo-butyl)-cyclohexa-2,5-dienecarboxylic acid methyl ester(80900-60-3)
EPA Substance Registry System: 2-(tert-Butyl-dimethyl-silanyloxy)-6-methoxy-1-(3-oxo-butyl)-cyclohexa-2,5-dienecarboxylic acid methyl ester(80900-60-3)

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: 80900-60-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 80900-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,0 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 80900-60:
(7*8)+(6*0)+(5*9)+(4*0)+(3*0)+(2*6)+(1*0)=113
113 % 10 = 3
So 80900-60-3 is a valid CAS Registry Number.

80900-60-3Upstream product

80900-55-6 methyl 2-(t-butyldimethylsiloxy)-6-methoxybenzoate

80900-60-3Downstream Products

80900-60-3Relevant academic research and scientific papers

STUDIES ON REDUCTIVE ALKYLATION: SYNTHESIS OF WIELAND-MIESCHER KETONE ANALOGUES BEARING AN OXYGENATED ANGULAR SUBSTITUENT

Mander, L. N.,Hamilton, R. J.

, p. 4115 - 4118 (2007/10/02)

Wieland-Miescher analogues 2a and 2b have been prepared in good yield by a sequence utilising reductive alkylation of the dihydro aromatic ester enolate 7d, which functions as a synthetic equivalent of the dioxo ester 5 anion; these analogues are envisaged as intermediates in a projected synthesis of bruceantin.

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