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(E)-N-phenyl-2-cyclohexyl-2-nonenamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136583-52-3

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136583-52-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136583-52-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,5,8 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 136583-52:
(8*1)+(7*3)+(6*6)+(5*5)+(4*8)+(3*3)+(2*5)+(1*2)=143
143 % 10 = 3
So 136583-52-3 is a valid CAS Registry Number.

136583-52-3Downstream Products

136583-52-3Relevant academic research and scientific papers

Reaction of Tantalum-Alkyne Complexes with Isocyanates or Acyl Cyanides. Stereoselective Functionalization of Carbon-Carbon Triple Bonds

Kataoka, Yasutaka,Oguchi, Yoshiyuki,Yoshizumi, Kazuyuki,Miwatashi, Seiji,Takai, Kazuhiko,Utimoto, Kiitiro

, p. 1543 - 1549 (2007/10/02)

Treatment of alkynes with low-valent tantalum derived from TaCl5 and zinc produces tantalum-alkyne complexes (not isolated), which react in situ with phenyl isocyanate (or butyl isocyanate) to give (E)-α,β-unsaturated amides stereoselectively.The tantalum-alkyne complexes also react with acyl cyanides in the presence of BF3*OEt2 to give α-cyanohydrins.In both reactions, filtration of the reaction mixture containing the tantalum-alkyne complexes before addition of isocyanates (or acyl cyanides) is indispensable to obtain good yields.

Reaction of Tantalum-Alkyne Complexes with Isocyanates Leading to (E)-α,β-Unsaturated Amides. Stereoselective Functionalization of Carbon-Carbon Triple Bonds

Takai, Kazuhiko,Kataoka, Yasutaka,Yoshizumi, Kazuyuki,Oguchi, Yoshiyuki,Utimoto, Kiitiro

, p. 1479 - 1482 (2007/10/02)

Treatment of alkynes with low-valent tantalum derived from TaCl5 and zinc produces tantalum-alkyne complexes (not isolated), which react with phenylisocyanate (or butylisocyanate) to give (E)-α,β-unsaturated amides stereoselectively.

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