Cas 533909-12-5,3-(S)-2-acryloyl-3-(tert-butyldimethylsilanyloxymethyl)-3-methylpent-4-enoic acid ethyl ester

533909-12-5

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Basic information

Product Name: 3-(S)-2-acryloyl-3-(tert-butyldimethylsilanyloxymethyl)-3-methylpent-4-enoic acid ethyl ester
Synonyms: 3-(S)-2-acryloyl-3-(tert-butyldimethylsilanyloxymethyl)-3-methylpent-4-enoic acid ethyl ester
CAS NO:533909-12-5
Molecular Formula:
Molecular Weight: 340.535
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: 3-(S)-2-acryloyl-3-(tert-butyldimethylsilanyloxymethyl)-3-methylpent-4-enoic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-(S)-2-acryloyl-3-(tert-butyldimethylsilanyloxymethyl)-3-methylpent-4-enoic acid ethyl ester(533909-12-5)
EPA Substance Registry System: 3-(S)-2-acryloyl-3-(tert-butyldimethylsilanyloxymethyl)-3-methylpent-4-enoic acid ethyl ester(533909-12-5)

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: 533909-12-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 533909-12-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,3,9,0 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 533909-12:
(8*5)+(7*3)+(6*3)+(5*9)+(4*0)+(3*9)+(2*1)+(1*2)=155
155 % 10 = 5
So 533909-12-5 is a valid CAS Registry Number.

533909-12-5Upstream product

533909-11-4 3-(S)-3-(tert-butyldimethylsilanyloxymethyl)-3-methyl-2-(3-phenylsulfanylpropionyl)pent-4-enoic acid ethyl ester

533909-12-5Downstream Products

533909-12-5Relevant academic research and scientific papers

Pd-catalyzed asymmetric allylic alkylation. A short route to the cyclopentyl core of viridenomycin

Trost, Barry M.,Jiang, Chunhui

, p. 1563 - 1565 (2003)

(Matrix presented) A palladium-catalyzed asymmetric allylic alkylation effects a dynamic kinetic asymmetric transformation of racemic isoprene monoepoxide and a surrogate for Nazarov's reagent in which a quaternary center is created with exellent ee. The

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