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13151-29-6

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13151-29-6 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 70, p. 3342, 1948 DOI: 10.1021/ja01190a036

Check Digit Verification of cas no

The CAS Registry Mumber 13151-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,5 and 1 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13151-29:
(7*1)+(6*3)+(5*1)+(4*5)+(3*1)+(2*2)+(1*9)=66
66 % 10 = 6
So 13151-29-6 is a valid CAS Registry Number.

13151-29-6Relevant articles and documents

BIS(ALK-4-ENYL)ZINK-VERBINDUNGEN DURCH ADDITION VON ALK-2-ENYLZINK AN OLEFINE

Lehmkuhl, Herbert,Doering, Ingo,Nehl, Hans

, p. 123 - 130 (1981)

The dialk-2-enylzinc compounds I-IV add to ethylene, oct-1-ene and 3,3-dimethylcyclopropene to give the corresponding di-alk-4-enylzinc compounds VI-IX (88-98percent yield), XV and XVI (90-94percent yield), XVII (7percent) and XXIIIa-XXVIa (91-98percent yield).Additions to XIII are regioselective with Zn -> C(1) while stereoselective cis-addition to XXII is observed.

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Letsinger,Traynham

, p. 849,851 (1950)

-

Cu-Catalyzed cascades to carbocycles: Union of diaryliodonium salts with alkenes or alkynes exploiting remote carbocations

Zhang, Fengzhi,Das, Shoubhik,Walkinshaw, Andrew J.,Casitas, Alicia,Taylor, Michael,Suero, Marcos G.,Gaunt, Matthew J.

supporting information, p. 8851 - 8854 (2014/07/08)

Copper-catalyzed cascade reactions between alkenes or alkynes and diaryliodonium salts form carbocyclic products in a single step. Arylation of the unsaturated functional group is proposed to form a carbocation intermediate that facilitates hydride shift pathways to translocate the positive charge to a remote position and enables ring formation via a Friedel-Crafts-type reaction.

Copper-catalyzed allylation of alkyl halides with allylic grignard reagents

Sai, Masahiro,Yorimitsu, Hideki,Oshima, Koichiro

experimental part, p. 1194 - 1196 (2009/12/25)

Treatment of alkyl halides, including secondary and tertiary alkyl bromides, with allylic Grignard reagents in the presence of a catalytic amount of copper(II) triflate in diisopropyl ether at 25 °C yielded the corresponding allylated products in high yie

All-catalytic, efficient, and asymmetric synthesis of α,ω- diheterofunctional reduced polypropionates via "one-pot" Zr-catalyzed asymmetric carboalumination - Pd-catalyzed cross-coupling tandem process

Novak, Tibor,Tan, Ze,Liang, Bo,Negishi, Ei-Ichi

, p. 2838 - 2839 (2007/10/03)

A highly efficient method for the synthesis of stereochemically pure (≥99% ee and >50/1 dr) α,ω-diheterofunctional reduced polypropionates has been developed. The essential features of the method are represented by the conversion of inexpensive styrene in

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