Cas 81617-03-0,[4-(2-Methoxy-ethoxymethoxy)-2-methylene-3-phenyl-butyl]-trimethyl-silane

81617-03-0

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Basic information

Product Name: [4-(2-Methoxy-ethoxymethoxy)-2-methylene-3-phenyl-butyl]-trimethyl-silane
Synonyms: [4-(2-Methoxy-ethoxymethoxy)-2-methylene-3-phenyl-butyl]-trimethyl-silane
CAS NO:81617-03-0
Molecular Formula:
Molecular Weight: 322.52
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: [4-(2-Methoxy-ethoxymethoxy)-2-methylene-3-phenyl-butyl]-trimethyl-silane(CAS DataBase Reference)
NIST Chemistry Reference: [4-(2-Methoxy-ethoxymethoxy)-2-methylene-3-phenyl-butyl]-trimethyl-silane(81617-03-0)
EPA Substance Registry System: [4-(2-Methoxy-ethoxymethoxy)-2-methylene-3-phenyl-butyl]-trimethyl-silane(81617-03-0)

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: 81617-03-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 81617-03-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,1 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 81617-03:
(7*8)+(6*1)+(5*6)+(4*1)+(3*7)+(2*0)+(1*3)=120
120 % 10 = 0
So 81617-03-0 is a valid CAS Registry Number.

81617-03-0Upstream product

81617-03-0Downstream Products

81617-04-1 4-Methylene-3-phenyl-tetrahydro-pyran

81617-03-0Relevant academic research and scientific papers

Reaction of 2-Methoxyethyl Hemiacetals with Allylsilanes in the Presence of Titanium Tetrachloride: Regioselective C-O Bond Cleavage of the Unsymmetrical Acetals

Nishiyama, Hisao,Itoh, Kenji

, p. 2496 - 2498 (1982)

Reaction of 2-methoxyethyl hemiacetals with allylsilanes in the presence of titanium tetrachloride gave the corresponding homoallyl ethers in good yields by the regioselective C-O bond cleavage of the hemiacetals.A new carbon homologative cyclization was

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