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3-benzyl-1-methylpiperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85237-73-6

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85237-73-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85237-73-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,2,3 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85237-73:
(7*8)+(6*5)+(5*2)+(4*3)+(3*7)+(2*7)+(1*3)=146
146 % 10 = 6
So 85237-73-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H19N/c1-14-9-5-8-13(11-14)10-12-6-3-2-4-7-12/h2-4,6-7,13H,5,8-11H2,1H3

85237-73-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-benzyl-1-methylpiperidine

1.2 Other means of identification

Product number -
Other names Piperidine,1-methyl-3-(phenylmethyl)

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:85237-73-6 SDS

85237-73-6Downstream Products

85237-73-6Relevant academic research and scientific papers

Synthesis of ruthenium N-heterocyclic carbene complexes and their catalytic activity for β-alkylation of tertiary cyclic amines

?zdemir, Ismail,Dü?ünceli, Serpil Demir,Kalo?lu, Nazan,Achard, Mathieu,Bruneau, Christian

, p. 311 - 315 (2015)

The novel ruthenium N-Heterocyclic carbene complexes are synthesized, and characterized by studying its 1H, 13C, elemental analysis, and X-ray. These complexes have been reported as promising catalyst for β C-H bond functionalization of tertiary cyclic amines through hydrogen autotransfers in the presence of external acidic additive. The new catalytic products were characterized by 1H NMR, 13C NMR spectroscopic methods.

N-heterocyclic carbene based ruthenium complexes for selective β-C(sp3)-H functionalization of N-fused saturated cyclic amines

Kalo?lu, Nazan

, p. 2265 - 2272 (2019/03/13)

Herein, a series of new ruthenium(II) complexes with the general molecular formula [RuCl2(arene)(NHC)], (arene = η6-p-cymene, NHC = N-heterocyclic carbene) were synthesized from in situ prepared silver(I)-NHCs by the transmetallation method. These complexes were fully characterized by analytical and spectral methods. Ruthenium(II) complexes were tested as promising catalyst for selective β-C(sp3)-H functionalization of N-methylpiperidine with various aldehydes through hydrogen transfers in presence of external acidic additive. These eco-friendly cross-dehydrogenative couplings enable the production of C(3)-alkylated N-methylpiperidine derivatives without enamines with only carbon dioxide and water as benign by-product.

Ruthenium(II) and iridium(III) complexes featuring NHC-sulfonate chelate

Rajaraman,Sahoo,Hild,Fischmeister,Achard,Bruneau

, p. 17467 - 17472 (2015/10/19)

Three new complexes bearing a chelating (κ2C,O) NHC-SO3 ligand have been prepared. An original method for the synthesis of the imidazolium-sulfonate NHC precursor is described. The 5-membered ruthena- and irida-cycle containing complexes were fully characterized and evaluated in a series of catalytic transformations involving hydrogen auto-transfer processes.

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