Cas 129261-46-7,(S)-3-((2S,3R)-3-Benzyloxymethyl-oxiranyl)-3-(dimethyl-phenyl-silanyl)-propionic acid methyl ester

129261-46-7

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Basic information

Product Name: (S)-3-((2S,3R)-3-Benzyloxymethyl-oxiranyl)-3-(dimethyl-phenyl-silanyl)-propionic acid methyl ester
Synonyms:
CAS NO:129261-46-7
Molecular Formula:
Molecular Weight: 384.547
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: (S)-3-((2S,3R)-3-Benzyloxymethyl-oxiranyl)-3-(dimethyl-phenyl-silanyl)-propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-3-((2S,3R)-3-Benzyloxymethyl-oxiranyl)-3-(dimethyl-phenyl-silanyl)-propionic acid methyl ester(129261-46-7)
EPA Substance Registry System: (S)-3-((2S,3R)-3-Benzyloxymethyl-oxiranyl)-3-(dimethyl-phenyl-silanyl)-propionic acid methyl ester(129261-46-7)

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: 129261-46-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129261-46-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,2,6 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 129261-46:
(8*1)+(7*2)+(6*9)+(5*2)+(4*6)+(3*1)+(2*4)+(1*6)=127
127 % 10 = 7
So 129261-46-7 is a valid CAS Registry Number.

129261-46-7Upstream product

128625-92-3 (E)-(S)-6-Benzyloxy-3-(dimethyl-phenyl-silanyl)-hex-4-enoic acid methyl ester

129261-46-7Downstream Products

129261-46-7Relevant academic research and scientific papers

Allylsilanes in organic synthesis; stereoselective preparation and reactions of functionalised β,γ-epoxysilanes

Murphy, Patrick J.,Russell, Andrew T.,Procter, Garry

, p. 1055 - 1058 (1990)

Epoxidation of ester-allylsilanes such as (1) after alkylation adjacent to the carbonyl group produces the corresponding epoxides with high diastereoselectivity.

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