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46230-01-7

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46230-01-7 Usage

General Description

Furan-2-ylmethyl-pyridin-2-yl-amine hydrochloride is a chemical compound that consists of a furan ring attached to a pyridine ring with a methyl group on the furan ring and an amine group on the pyridine ring. It is typically found in the form of a hydrochloride salt. FURAN-2-YLMETHYL-PYRIDIN-2-YL-AMINE HYDROCHLORIDE has potential applications in the pharmaceutical industry, particularly in the development of new drugs and medications. It may also have uses in chemical research and synthesis due to its unique chemical structure and reactivity. However, further research and testing are necessary to fully understand the potential uses and properties of furan-2-ylmethyl-pyridin-2-yl-amine hydrochloride.

Check Digit Verification of cas no

The CAS Registry Mumber 46230-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,2,3 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 46230-01:
(7*4)+(6*6)+(5*2)+(4*3)+(3*0)+(2*0)+(1*1)=87
87 % 10 = 7
So 46230-01-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O/c1-2-6-11-10(5-1)12-8-9-4-3-7-13-9/h1-7H,8H2,(H,11,12)

46230-01-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(furan-2-ylmethyl)pyridin-2-amine,hydrochloride

1.2 Other means of identification

Product number -
Other names furan-2-ylmethyl-pyridin-2-yl-amine

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:46230-01-7 SDS

46230-01-7Downstream Products

46230-01-7Relevant articles and documents

Furfural and 5-(hydroxymethyl)furfural valorization using homogeneous Ni(0) and Ni(II) catalysts by transfer hydrogenation

Arévalo, Alma,García, Juventino J.,Jurado-Vázquez, Tamara

supporting information, (2021/11/27)

The complex [dippeNi(COD)] (dippe =1,2-bis(diisopropyl phosphino)ethane) was used as a catalytic precursor in furfural (FF) and 5-(hydroxymethyl)furfural (HMF) valorization, along with formic acid as hydrogen transfer agent, to produce the corresponding a

Half-sandwich Ru(ii) arene complexes bearing benzimidazole ligands for theN-alkylation reaction of aniline with alcohols in a solvent-free medium

?i?ek, Metin,Gürbüz, Nevin,?zdemir, Nam?k,?zdemir, ?smail,?spir, Esin

, p. 11075 - 11085 (2021/07/02)

In this article, the directN-alkylation reactions of amines with alcohol derivatives using the borrowing hydrogen methodology have been investigated. For this purpose, a new series of half-sandwich ruthenium(ii) complexes bearing N-coordinated benzimidazole complexes have been synthesized and fully characterized by FT-IR,1H NMR and13C NMR spectroscopies. Additionally, the structures of the complexes2a-2ehave been characterized by X-ray crystallography. All new complexes were investigated for their catalytic activities in the alkylation reaction of amines with alcohol derivatives. It was found that alkylation reactions in a solvent-free medium are efficient and selective.

First used of Alkylbenzimidazole-Cobalt(II) complexes as a catalyst for the N-Alkylation of amines with alcohols under solvent-free medium

?zdemir, ?smail,?zdemir, Nam?k,?ahin, Neslihan,Gürbüz, Nevin,Y?ld?r?m, ?lkay

, (2020/04/28)

In this study, alkylbenzimidazole-cobalt(II)-catalyzed direct N-alkylation reactions of amines with alcohols derivatives have been investigated under solvent-free medium. For this purpose, a series of cobalt(II) complexes bearing N-alkylbenzimidazole complexes have been synthesized and novel complexes fully characterized by elemental analysis, FT-IR, 1H NMR and, 13C{1H} NMR spectroscopies. Also, the structure of the complex 2a has been confirmed by X-ray crystallography. Generally, the N-alkylating reaction is usually performed in toluene with various metal complexes including cobalt. In this catalytic study of complexes, 2a-c has carried out in without solvent and alcohol acted both as solvent and reactant. Conversion and selectivity of amine products according to imine products for alkylation reactions have been seen high yield in medium solvent-free relative to in toluene.

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