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

14044-90-7

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14044-90-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14044-90-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,0,4 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14044-90:
(7*1)+(6*4)+(5*0)+(4*4)+(3*4)+(2*9)+(1*0)=77
77 % 10 = 7
So 14044-90-7 is a valid CAS Registry Number.

14044-90-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(furan-2-ylmethyl)piperidine

1.2 Other means of identification

Product number -
Other names 2-Piperidinomethyl-furan

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:14044-90-7 SDS

14044-90-7Downstream Products

14044-90-7Relevant academic research and scientific papers

Hydrazone complexes of ruthenium(II): Synthesis, crystal structures and catalytic applications in N-alkylation reactions

Murugan, Kaliyappan,Natarajan, Karuppannan,Nirmala, Muthukumaran,Vijayapritha, Subbarayan,Viswanathamurthi, Periasamy

, (2020)

A series of new Ru(II) complexes of 8-hydroxy quinoline-2-carboxyaldehyde hydrazone of the general formula [RuH(CO)(EPh3)2L] (1–6) (E = P or As, L = N’-((8-hydroxyquinolin-2-yl)methylene)thiophene-2-carbohydrazide (HQ-THy), N’-((8-hydroxyquinolin-2-yl)methylene)isonicotinohydrazide (HQ-IHy), N’-((8-hydroxyquinolin-2-yl)methylene) benzohydrazide (HQ-BHy)) have been synthesized. They have been characterized by elemental analysis, IR, NMR (1H, 13C & 31P) and ESI-MS spectral methods. Further, structures of two of the complexes have been determined by single crystal X-ray diffraction technique which revealed a pseudo octahedral geometry with the coordination of the quinoline nitrogen and quinoline oxygen atoms of the ligand. All the new complexes have been employed as efficient catalysts in N-alkylation reactions for the synthesis of tertiary amines by the coupling of secondary amines with aromatic primary alcohols at low catalyst loading with maximum yields. In addition, the effects of substituents on the ligands, different solvents as well as bases and amounts of catalyst loading on the catalytic activity of the complexes have been thoroughly investigated. Complex 1 was found to be efficient catalyst towards N-alkylation of alcohols with the amine. Further, a variety of secondary amines and aromatic (hetero) primary alcohols with various functional groups have also been successfully used in the N-alkylation reactions and it has been found that only one equivalent of the alcohol was consumed in the process.

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