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(E)-1-phenylsulfanyl-1-trimethylsilyl-1-octene is a complex organic compound characterized by its unique structure and properties. It features an octene chain with a trimethylsilyl group at the 1-position and a phenylsulfanyl group at the same position, indicating a (E)-configuration. (E)-1-phenylsulfanyl-1-trimethylsilyl-1-octene is known for its stability and reactivity, which can be attributed to the presence of the trimethylsilyl group, a common protecting group in organic synthesis, and the phenylsulfanyl group, which can participate in various chemical reactions. The compound's structure allows for potential applications in the synthesis of more complex molecules and may be of interest in the fields of pharmaceuticals, materials science, and chemical research.

87514-04-3

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87514-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87514-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,1 and 4 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 87514-04:
(7*8)+(6*7)+(5*5)+(4*1)+(3*4)+(2*0)+(1*4)=143
143 % 10 = 3
So 87514-04-3 is a valid CAS Registry Number.

87514-04-3Downstream Products

87514-04-3Relevant articles and documents

A facile stereoselective synthesis of (E)-α-silylyinyl sulfides via hydromagnesiation of alkynylsilanes

Cai, Mingzhong,Xia, Jim,Wang, Pingping

, p. 644 - 647 (2005)

Hydromagnesiation of alkynylsilanes 1 in diethyl ether gave (Z)-α-silylvinyl Grignard reagents 2, which reacted with arylsulfenyl chlorides 3 to afford stereoselectively (E)-α-silylvinyl sulfides 4 in good yields. (E)-α-Silylvinyl sulfides 4 could undergo

Stereo-recognizing transformation of (E)-alkenyl halides into sulfides catalyzed by nickel(0) triethyl phosphite complex

Yatsumonji, Yasutaka,Okada, Orie,Tsubouchi, Akira,Takeda, Takeshi

, p. 9981 - 9987 (2007/10/03)

(E)-Alkenyl halides were transformed into (E)-alkenyl sulfides by the nickel(0) triethyl phosphite complex-catalyzed reaction with thiols, whereas (Z)-alkenyl halides gave alkynes under the same reaction conditions. Aryl halides were also transformed into aryl sulfides using the same reagent system.

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