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Benzene, (1-hexenylsulfinyl)-, (Z)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138286-21-2

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138286-21-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138286-21-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,2,8 and 6 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 138286-21:
(8*1)+(7*3)+(6*8)+(5*2)+(4*8)+(3*6)+(2*2)+(1*1)=142
142 % 10 = 2
So 138286-21-2 is a valid CAS Registry Number.

138286-21-2Downstream Products

138286-21-2Relevant academic research and scientific papers

Stereoselective synthesis of (E)-Vinyl Sulfoxides by the Horner-Wittig reaction

Van Steenis, Jan Hein,Van Es, Joseph Johannes Gerardus Steven,Van Der Gen, Arne

, p. 2787 - 2793 (2007/10/03)

The Horner-Wittig reaction of sulfinylmethyl-substituted di-phenylphosphane oxides 1-3 with aldehydes is reported. In a straightforward synthesis, (E)-vinyl sulfoxides 4 (R1 = Ph), 5 (R1 = Me) and 6 (R1=pTol) were formed m

Hydrozirconation of alkynyl sulfoxides: The reactions of zirconated vinyl sulfoxide intermediates

Zhong, Ping,Huang, Xian,Ping-Guo, Meng

, p. 8921 - 8925 (2007/10/03)

Alkynyl sulfoxides react with Cp2Zr(H)Cl in THF at room temperature to give the α-zirconated and β-zirconated vinyl sulfoxides, which react with a wide range of electrophiles to give several types of di- or trisubstituted olefins, such as Z-vinyl sulfoxides and α- or β-halo vinyl sulfoxides. (C) 2000 Elsevier Science Ltd.

Reactions of 2-Halovinyl Aryl Sulfoxides with Organometallic Reagents

Cardellicchio, Cosimo,Fiandanese, Vito,Naso, Francesco

, p. 1718 - 1722 (2007/10/02)

(E)- and (Z)-halovinyl aryl sulfoxides 1-4 were subjected to reactions with organocopper, organomagnesium, or organolithium reagents.The organometallic reagents gave different products: diorganocuprates led to formation of carbon-carbon bond, with production of alkenyl sulfoxides 5-10, whereas formation of carbon-sulfur bond and production of diaryl or aryl alkyl sulfoxides 11-13 were observed in the reaction with the other organometallics.Possible mechanisms for the two observed processes are briefly discussed.

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