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Piperidine, 1-(3-cyclohexyl-2-propenyl)-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85972-81-2

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85972-81-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85972-81-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,9,7 and 2 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 85972-81:
(7*8)+(6*5)+(5*9)+(4*7)+(3*2)+(2*8)+(1*1)=182
182 % 10 = 2
So 85972-81-2 is a valid CAS Registry Number.

85972-81-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name piperidino-3 cyclohexyl-1 propene-1 trans

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:85972-81-2 SDS

85972-81-2Downstream Products

85972-81-2Relevant academic research and scientific papers

Cationic [(Iminophosphine)Nickel(Allyl)]+Complexes as the First Example of Nickel Catalysts for Direct Hydroamination of Allenes

Tafazolian, Hosein,Schmidt, Joseph A. R.

, p. 1507 - 1511 (2017)

The first example of nickel-catalyzed hydroamination of allenes is reported. The new cationic [(3-iminophosphine)nickel(allyl)]+catalysts have been fully characterized and act regioselectively in the catalytic hydroamination of allenes with sec

Electronic role of 3-iminophosphine ligands in palladium-catalyzed intermolecular hydroamination

Tafazolian, Hosein,Samblanet, Danielle C.,Schmidt, Joseph A.R.

, p. 1809 - 1817 (2015)

This study of the electronic characteristics of (3-iminophosphine)allylpalladium triflate complexes has yielded catalysts with moderate to high activity for the hydroamination of monosubstituted allenes utilizing a wide range of amines. Herein, a new seri

HYDROBORATION D'AMINES INSATUREES-II REGIO ET STEREOSELECTIVITE DE L'HYDROBORATION-ALKYLATION D'AMINES ACETYLENIQUES

Torregrosa, J. L.,Baboulene, M.,Speziale, V.,Lattes, A.

, p. 2355 - 2363 (2007/10/02)

The hydroboration reaction of acetylenic amines R1R2N-CH(R3)-CC-R4 was studied.We report the first results of a study of the reactivity of dialkylborane R2BH towards these amines which allow us to propose a new method for the synthesis of differently substituted β-ethylenic amines.The regioselectivity and the stereoselectivity of this reaction are examined and allow us to set out the possibility of a trans hydroboration.

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