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63430-96-6

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63430-96-6 Usage

General Description

2-hydroxyMethyl-1,2,3,4-tetrahydroquinoline is a chemical compound that falls under the category of tetrahydroquinolines. It is an organic compound with a molecular formula C10H13NO, and it contains a hydroxymethyl group and a tetrahydroquinoline ring. This chemical has been studied for potential applications in medicinal chemistry, particularly in the development of new drugs and pharmaceuticals. It may also have potential use in the field of materials science due to its unique structure and properties. However, further research is needed to fully understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 63430-96-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,4,3 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63430-96:
(7*6)+(6*3)+(5*4)+(4*3)+(3*0)+(2*9)+(1*6)=116
116 % 10 = 6
So 63430-96-6 is a valid CAS Registry Number.

63430-96-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxymethyl-1,2,3,4-tetrahydroquinoline

1.2 Other means of identification

Product number -
Other names (S)-(1,2,3,4-Tetrahydroquinolin-2-yl)methanol

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:63430-96-6 SDS

63430-96-6Relevant articles and documents

Consecutive Intermolecular Reductive Amination/Asymmetric Hydrogenation: Facile Access to Sterically Tunable Chiral Vicinal Diamines and N-Heterocyclic Carbenes

Chen, Ya,Pan, Yixiao,He, Yan-Mei,Fan, Qing-Hua

, p. 16831 - 16834 (2019/11/13)

A highly enantioselective iridium- or ruthenium-catalyzed intermolecular reductive amination/asymmetric hydrogenation relay with 2-quinoline aldehydes and aromatic amines has been developed. A broad range of sterically tunable chiral N,N′-diaryl vicinal diamines were obtained in high yields (up to 95 %) with excellent enantioselectivity (up to >99 % ee). The resulting chiral diamines could be readily transformed into sterically hindered chiral N-heterocyclic carbene (NHC) precursors, which are otherwise difficult to access. The usefulness of this synthetic approach was further demonstrated by the successful application of one of the chiral vicinal diamines and chiral NHC ligands in a transition-metal-catalyzed asymmetric Suzuki–Miyaura cross-coupling reaction and asymmetric ring-opening cross-metathesis, respectively.

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