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N-benzyl-1-(4-chlorophenyl)-3-butenylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

111865-49-7

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111865-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 111865-49-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,8,6 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 111865-49:
(8*1)+(7*1)+(6*1)+(5*8)+(4*6)+(3*5)+(2*4)+(1*9)=117
117 % 10 = 7
So 111865-49-7 is a valid CAS Registry Number.

111865-49-7Downstream Products

111865-49-7Relevant academic research and scientific papers

Allylstannane Allylation of Aldimines Activated by Chlorotrimethylsilane

Wang, De-Kun,Dai, Li-Xin,Hou, Xue-Long

, p. 8649 - 8652 (1995)

Aldimines activated by chlorotrimethylsilane reacted with allylstannane to give the corresponding homoallylic amines with excellent yields.

Allylation of Imines with in situ Generated Allyl Lead Reagents in a PbBr2/Al/BF3*OEt2/Et2O System

Tanaka, Hideo,Yamashita, Shiro,Ikemoto, Youichi,Torii, Sigeru

, p. 673 - 674 (1987)

Reductive addition of allyl bromide to imines has been performed with a combination of a catalytic amount of PbBr2 (0.03-0.1 equiv.) and Al (1 equiv.) in Et2O containing BF3*OEt2 (1.1 equiv.).

Mg and Zn mediated allylation of imines with allyl bromide

Wang, De-Kun,Dai, Li-Xin,Hou, Xue-Long,Zhang, Yi

, p. 4187 - 4188 (1996)

Both aldimines and ketamines are allylated under simple Barbier-type conditions using allyl bromide and commercial magnesium foil or zinc dust in tetrahydrofuran at room temperature.

A three-component synthesis of homoallylic amines catalyzed by CuI

Kalita, Pabitra Kumar,Phukan, Prodeep

, p. 5495 - 5497 (2008/12/22)

Cuprous iodide is a very effective catalyst for the three-component condensation of an aldehyde, benzylamine and allyltributylstannane in DMF to produce homoallylic amines in high yields.

Indium mediated Barbier-type allylation of aldimines in alcoholic solvents

Vilaivan, Tirayut,Winotapan, Chutima,Shinada, Tetsuro,Ohfune, Yasufumi

, p. 9073 - 9076 (2007/10/03)

Barbier-type allylation of unactivated aldimines with allyl bromides in the presence of indium powder took place rapidly in alcoholic solvents to give homoallylic amines in fair to good yields.

A NOVEL "Ti(0)" INDUCED ALLYLATION OF AMINES IN A TiCl4 (cat.)/ Al BIMETAL SYSTEM. CHIRALITY TRANSFER OF l-VALINE TO HOMOALLYLAMINE

Tanaka, Hideo,Inoue, Keizo,Pokorski, Ulrike,Taniguchi, Masatoshi,Torii, Sigeru

, p. 3023 - 3026 (2007/10/02)

"Barbier Type" allylation of imines with allyl bromide has been performed successfully by the action of aluminium (1 equiv.) and titanium(IV) chloride (0.05 equiv.) in THF.The chirality transfer of α-amino acid esters to homoallyl amines is demonstrated b

ELECTROREDUCTIVE "BARBIER TYPE" ALLYLATION OF IMINES WITH A COMBINATION OF A Pb(O)/Pb(II) REDOX MEDIATOR AND SACRIFICAL ANODE (Al)

Tanaka, Hideo,Nakahara, Takao,Dhimane, Hamid,Torii, Sigeru

, p. 4161 - 4164 (2007/10/02)

An electroreductive "Barbier Type" allylation of imines with allyl bromide has been performed in a PbBr2/Bu4NBr/THF-(Al anode)-(Pt cathode) system.A combination of Pb(O)/Pb(II) redox and a sacrifical aluminum anode works as a madiator for both cathodic an

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