Cas 932718-88-2,[(1S,2S,3R)-2-(4-methoxybenzyloxy)-1-methoxymethyl-3-methyl-4-hexynyl]oxy(triisopropyl)silane

932718-88-2

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Basic information

Product Name: [(1S,2S,3R)-2-(4-methoxybenzyloxy)-1-methoxymethyl-3-methyl-4-hexynyl]oxy(triisopropyl)silane
Synonyms: [(1S,2S,3R)-2-(4-methoxybenzyloxy)-1-methoxymethyl-3-methyl-4-hexynyl]oxy(triisopropyl)silane
CAS NO:932718-88-2
Molecular Formula:
Molecular Weight: 448.718
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: [(1S,2S,3R)-2-(4-methoxybenzyloxy)-1-methoxymethyl-3-methyl-4-hexynyl]oxy(triisopropyl)silane(CAS DataBase Reference)
NIST Chemistry Reference: [(1S,2S,3R)-2-(4-methoxybenzyloxy)-1-methoxymethyl-3-methyl-4-hexynyl]oxy(triisopropyl)silane(932718-88-2)
EPA Substance Registry System: [(1S,2S,3R)-2-(4-methoxybenzyloxy)-1-methoxymethyl-3-methyl-4-hexynyl]oxy(triisopropyl)silane(932718-88-2)

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: 932718-88-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 932718-88-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,2,7,1 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 932718-88:
(8*9)+(7*3)+(6*2)+(5*7)+(4*1)+(3*8)+(2*8)+(1*8)=192
192 % 10 = 2
So 932718-88-2 is a valid CAS Registry Number.

932718-88-2Upstream product

824-94-2 p-methoxybenzyl chloride

932718-88-2Downstream Products

932718-42-8 [(1S,2S,3R)-5-iodo-2-(4-methoxybenzyloxy)-1-methoxymethyl-3-methyl-4(E)-hexenyl]oxy(triisopropyl)silane

932718-88-2Relevant academic research and scientific papers

Crotylation versus propargylation: Two routes for the synthesis of the C13-C18 fragment of the antibiotic branimycin

Felzmann, Wolfgang,Castagnolo, Daniele,Rosenbeiger, Daniela,Mulzer, Johann

, p. 2182 - 2186 (2007)

The C13-C18 fragment 3 of the novel antibiotic branimycin was prepared along two highly stereocontrolled routes. The first one uses a standard Roush crotylation protocol, whereas the second one proceeds via an allenyl silane propargylation with unexpected stereochemical consequences, which are discussed in detail.

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