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39217-93-1

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39217-93-1 Usage

General Description

8-NITRO-1,2,3,4-TETRAHYDROQUINOLINE is a chemical compound with the molecular formula C9H10N2O2. It is a nitro-substituted tetrahydroquinoline compound with a yellow-brown crystalline appearance. 8-NITRO-1,2,3,4-TETRAHYDROQUINOLINE is used in the synthesis of various pharmaceuticals and can also be used as an intermediate in organic synthesis. It has potential applications in medicinal chemistry due to its various biological activities, such as antioxidant and anti-inflammatory properties. 8-NITRO-1,2,3,4-TETRAHYDROQUINOLINE undergoes various chemical reactions and can be used in the development of new drugs and therapies. Further research and studies on this compound may lead to its potential use in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 39217-93-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,2,1 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 39217-93:
(7*3)+(6*9)+(5*2)+(4*1)+(3*7)+(2*9)+(1*3)=131
131 % 10 = 1
So 39217-93-1 is a valid CAS Registry Number.

39217-93-1SDS

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 8-Nitro-1,2,3,4-tetrahydroquinoline

1.2 Other means of identification

Product number -
Other names 8-nitro-1,2,3,4-tetrahydro-quinoline

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:39217-93-1 SDS

39217-93-1Downstream Products

39217-93-1Relevant articles and documents

NHC-Palladium(II) Mononuclear and Binuclear Complexes Containing Phenylene-Bridged Bis(thione) Ligands: Synthesis, Characterization, and Catalytic Activities

Jia, Wei-Guo,Gao, Li-Li,Wang, Zhi-Bao,Wang, Jing-Jing,Sheng, En-Hong,Han, Ying-Feng

, p. 1790 - 1798 (2020)

A series of mono- and binuclear Pd(II) complexes with N-heterocyclic carbene (NHC) and phenylene-bridged bis(thione) (SCS) ligands were prepared and characterized by 1H and 13C NMR spectroscopy, IR, and mass spectrometry. The molecular structures of 1b, 2a, and 3b have been determined by the single-crystal X-ray diffraction method. The catalytic activities of the synthesized palladium complexes in the regioselective reduction of quinolines to the corresponding 1,2,3,4-tetrahydroquinolines were thoroughly investigated with ammonia-borane under mild reaction conditions. It is observed that the activities of the binuclear Pd(NHC) complexes were higher than those of the corresponding mononuclear complexes under the same conditions.

Cu Nanoclusters Anchored on the Metal-Organic Framework for the Hydrolysis of Ammonia Borane and the Reduction of Quinolines

Yun, Ruirui,Zhang, Beibei,Zhan, Feiyang,Du, Liting,Wang, Zhaoxu,Zheng, Baishu

supporting information, p. 12906 - 12911 (2021/08/30)

Free-access active sites created and the interaction regulated between them and substrates during the heterogeneous catalysis process are crucial, which remain a great challenge. In this work, in suit reduced to afford naked Cu nanoparticles (NPs) have been anchored on the metal-organic framework (MOF), NH2-MOF, to form Cu-NH2-MOF. The strategy can precisely control the Cu NP formation with small size and uniform distribution. The Cu NP properties and MOF advantages have been integrated to create a great catalyst with multiple functions and have resulted in improving the recyclability and superb catalytic activity for the one-pot reduction of heterocycle reactions under mild conditions. The experimental and theoretical calculation results show that the superior performance should be attributed to the framework of NH2-MOF that provides large caves for substrate enrichment and the stabilization of Cu sites by the -NH2 group.

High efficient iron-catalyzed transfer hydrogenation of quinolines with Hantzsch ester as hydrogen source under mild conditions

He, Renke,Cui, Peng,Pi, Danwei,Sun, Yan,Zhou, Haifeng

supporting information, p. 3571 - 3573 (2017/10/05)

A highly efficient transfer hydrogenation of quinolines with Hantzsch ester as hydrogen source in the presence of 1 mol% Fe(OTf)2 under mild conditions has been developed. A series of substituted 1,2,3,4-tetrahydroquinoline derivatives were afforded in excellent yields with good functional group tolerance.

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