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Trimethyl-((1E,4E)-4-phenylsulfanyl-hepta-1,4-dienyloxy)-silane is a complex organic compound with the molecular formula C14H22O2SSi. It is characterized by a unique structure that includes a trimethylsilyl group (Si(CH3)3), a conjugated diene system (1,4-diene), a phenylsulfanyl group (C6H5-S), and an ether linkage (-O-). Trimethyl-((1E,4E)-4-phenylsulfanyl-hepta-1,4-dienyloxy)-silane is of interest in organic synthesis and may be used as a reagent or intermediate in the preparation of various organic compounds, particularly those involving silicon or sulfur functionalities. Its specific applications can vary, but it is generally used to introduce or modify functional groups in target molecules, taking advantage of the reactivity of the diene, phenylsulfanyl, and silyl moieties.

80399-01-5

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80399-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80399-01-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,3,9 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80399-01:
(7*8)+(6*0)+(5*3)+(4*9)+(3*9)+(2*0)+(1*1)=135
135 % 10 = 5
So 80399-01-5 is a valid CAS Registry Number.

80399-01-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl(((4E)-4-(phenylthio)hepta-1,4-dien-1-yl)oxy)silane

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:80399-01-5 SDS

80399-01-5Relevant academic research and scientific papers

STRAIN AND SELECTIVITY: PARTNERS FOR ORGANIC SYNTHESIS

Trost, Barry M.

, p. 139 - 150 (2007/10/02)

The development of two new small-ring conjunctive reagents, (E)-2-(hydrohymethyl)cyclopropyl phenyl sulphide and 1,1-bis(benzenesulphonyl)cyclopropane, are reported.The former permits a synthesis of 2,4-disubstituted cyclobutanones and (E)-4-phenylthio-4-

Bifunctional Cyclopropyl Reagents: Stereocontrolled Approach to Vinyl Sulfides and Chemodifferentiated 1,4-Dicarbonyl Systems

Trost, Barry M.,Ornstein, Paul L.

, p. 748 - 751 (2007/10/02)

The use of (E)-2-(hydroxymethyl)cyclopropyl phenyl sulfide as a useful conjunctive reagent, particularly in a stereocontrolled synthesis of vinyl sulfides, is reported.

A CHEMOSELECTIVE DESULFURIZATION METHOD VIA HOMOGENEOUS NICKEL CATALYSIS

Trost, Barry M.,Ornstein, Paul L.

, p. 3463 - 3466 (2007/10/02)

Isopropylmagnesium bromide in the presence of bis-(triphenylphosphino)-nickel(II) chloride reduces vinyl sulfides stereospecifically to the corresponding olefins without overreduction - a process which serves as a key step in the synthesis of the sex pheromone of the Douglas fir tussock moth.

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