Cas 141352-35-4,(E)-(4S,5R)-4,5-Bis-benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-5-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-pent-2-enoic acid methyl ester

141352-35-4

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Basic information

Product Name: (E)-(4S,5R)-4,5-Bis-benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-5-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-pent-2-enoic acid methyl ester
Synonyms:
CAS NO:141352-35-4
Molecular Formula:
Molecular Weight: 556.772
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: (E)-(4S,5R)-4,5-Bis-benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-5-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-pent-2-enoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (E)-(4S,5R)-4,5-Bis-benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-5-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-pent-2-enoic acid methyl ester(141352-35-4)
EPA Substance Registry System: (E)-(4S,5R)-4,5-Bis-benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-5-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl)-pent-2-enoic acid methyl ester(141352-35-4)

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: 141352-35-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 141352-35-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,3,5 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141352-35:
(8*1)+(7*4)+(6*1)+(5*3)+(4*5)+(3*2)+(2*3)+(1*5)=94
94 % 10 = 4
So 141352-35-4 is a valid CAS Registry Number.

141352-35-4Upstream product

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141352-35-4Relevant academic research and scientific papers

Preparation of 1-methoxycarbonyl-1-t-butyldimethylsilyloxy epoxides. Their transformation into 3-hydroxy 2-acetal-esters and certain 3-hydroxy 2-keto-esters

Pujol, Bernard,Sabatier, Richard,Driguez, Pierre-Alexandre,Doutheau, Alain

, p. 1447 - 1450 (2007/10/02)

The peracid oxidation of methyl 2-(t-butyldimethylsilyloxy)-2-alkenoates 2 furnished the corresponding epoxides 3 in good yields. The regiospecific opening of the latter compounds with methanol afforded 3-hydroxy 2-acetal-esters 4. When alkyl disubstitute

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