Cas 886582-82-7,Triethyl-{(R)-3-methoxy-3-[(S)-1-(4-methoxy-benzyloxy)-ethyl]-penta-1,4-diynyl}-silane

886582-82-7

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Basic information

Product Name: Triethyl-{(R)-3-methoxy-3-[(S)-1-(4-methoxy-benzyloxy)-ethyl]-penta-1,4-diynyl}-silane
Synonyms: Triethyl-{(R)-3-methoxy-3-[(S)-1-(4-methoxy-benzyloxy)-ethyl]-penta-1,4-diynyl}-silane
CAS NO:886582-82-7
Molecular Formula:
Molecular Weight: 372.58
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: Triethyl-{(R)-3-methoxy-3-[(S)-1-(4-methoxy-benzyloxy)-ethyl]-penta-1,4-diynyl}-silane(CAS DataBase Reference)
NIST Chemistry Reference: Triethyl-{(R)-3-methoxy-3-[(S)-1-(4-methoxy-benzyloxy)-ethyl]-penta-1,4-diynyl}-silane(886582-82-7)
EPA Substance Registry System: Triethyl-{(R)-3-methoxy-3-[(S)-1-(4-methoxy-benzyloxy)-ethyl]-penta-1,4-diynyl}-silane(886582-82-7)

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: 886582-82-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 886582-82-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,6,5,8 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 886582-82:
(8*8)+(7*8)+(6*6)+(5*5)+(4*8)+(3*2)+(2*8)+(1*2)=237
237 % 10 = 7
So 886582-82-7 is a valid CAS Registry Number.

886582-82-7Upstream product

886582-82-7Downstream Products

886582-81-6 1-Methoxy-4-((1S,2R)-2-methoxy-1-methyl-4-triethylsilanyl-2-trimethylsilanylethynyl-but-3-ynyloxymethyl)-benzene

886582-82-7Relevant academic research and scientific papers

First asymmetric synthesis of a differentially silyl-protected tris(alkynyl)methyl methyl ether

Convertino, Vito,Manini, Peter,Schweizer, W. Bernd,Diederich, Francois

, p. 1206 - 1208 (2006)

The stereoselective synthesis of the differentially silyl-protected tris(alkynyl) methyl methyl ether, the first optically active trispropargylic alcohol derivative, was investigated. The asymmetric synthesis began with enantiometrically pure ethyl lactat

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