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(E)-1-phenyl-3-(phenyldimethylsiloxy)-2-butene is an organic compound characterized by a conjugated diene structure with a phenyl group at the 1-position and a phenyldimethylsiloxy group at the 3-position. This molecule features a double bond between the 2nd and 3rd carbon atoms, which is in the E configuration, indicating that the phenyl and phenyldimethylsiloxy groups are on opposite sides of the double bond. The phenyldimethylsiloxy group is a silicon-containing ether that can influence the reactivity and stability of the molecule. (E)-1-phenyl-3-(phenyldimethylsiloxy)-2-butene is of interest in organic synthesis, particularly in reactions involving silicon-based protecting groups and in the formation of complex organic structures.

86572-54-5

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86572-54-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86572-54-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,5,7 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86572-54:
(7*8)+(6*6)+(5*5)+(4*7)+(3*2)+(2*5)+(1*4)=165
165 % 10 = 5
So 86572-54-5 is a valid CAS Registry Number.

86572-54-5Downstream Products

86572-54-5Relevant academic research and scientific papers

Homobimetallic rhodium NHC complexes as versatile catalysts for hydrosilylation of a multitude of substrates in the presence of ambient air

Huckaba, Aron J.,Hollis, T. Keith,Reilly, Sean W.

, p. 6248 - 6256 (2013/12/04)

Two recently reported air- and water-stable di-Rh complexes based on 1,3-bis(3′-butylbenzimidazol-2′-ylidene)benzene were utilized as catalysts for hydrosilylation. Among the substrates investigated were aldehydes, ketones, α,β-unsaturated carbonyls, acyl chlorides, nitriles, alkenes, nitro groups, isocyanates, and tertiary amides. Additionally, carbon dioxide underwent hydrosilylation to produce dimethylphenylsilylformate. The catalysts compared well to other previously reported hydrosilylation catalysts, and the Rh-Cl catalyst was found to be faster and more selective than the Rh-I complex in each case.

Large-scale preparation and labelling reactions of deuterated silanes

Campos, Jesus,Rubio, Miguel,Esqueda, Ana C.,Carmona, Ernesto

experimental part, p. 29 - 38 (2012/06/30)

A catalytic synthesis of deuterated silanes SiEt3D, SiMe 2PhD and SiPh2D2 is reported that allows their facile generation in a 3-4g scale, utilizing D2 (0.5bar) as the hydrogen isotope source and low

Acylsilane chemistry. Synthesis of regio- and stereoisomerically defined enol silyl ethers using acylsilanes

Reich, Hans J.,Holtan, Ronald C.,Bolm, Carsten

, p. 5609 - 5617 (2007/10/02)

The preparation of enol silyl ethers using a carbonyl addition-Brook rearrangement-elimination sequence was studied. The key intermediate α-silyl-β-X-alkoxides could be prepared in several different ways, including the addition of organolithium or hydride reagents to α-X-acylsilanes (path a, using RM with R = alkyl, aryl, vinyl, alkynyl, silyl, stannyl, phosphinyl, and cyano), the addition of α-X-lithium reagents to acylsilanes (path b, X = phenylthio, phenylsulfonyl), or the addition of silyllithium reagents to α-X-ketones (path c, X = phenylthio, alkoxy). All of the reactions gave complete regiocontrol of silyl enol ether formation, and many gave excellent (>99%) stereocontrol as well. The selectivity of the carbonyl addition, silyl rearrangement, and elimination was studied. For path a, when the R group of RM was a poor carbanion stabilizing group the elimination of the intermediate α-silyl-β-X-alkoxides was stereospecific, and there was a large difference in rate between erythro and threo (erythro > threo). When R was a carbanion stabilizing group, such as aryl or alkynyl, the elimination process became nonstereospecific in some cases, and only small differences between threo and erythro were observed. Path b was especially effective with α-sulfonyl lithium reagents, and these reactions gave predominantly E enol silyl ethers (4/1 to 20/1). The addition of organolithium reagents to β-X-acylsilanes (the homologue of path a) was also briefly explored as a synthesis of siloxy-cyclopropanes.

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