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2051-28-7

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2051-28-7 Usage

Chemical Properties

clear colorless to light yellow low melting solid

Uses

Decahydroquinoline is a decahydroquinoline derivative with analgesic activity.

General Description

Hydrodenitrogenation of decahydroquinoline has been investigated over Ni-MoS2/γ-Al2O3 and NiMo(P)/Al2O3 catalysts.

Check Digit Verification of cas no

The CAS Registry Mumber 2051-28-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2051-28:
(6*2)+(5*0)+(4*5)+(3*1)+(2*2)+(1*8)=47
47 % 10 = 7
So 2051-28-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H17N/c1-2-6-9-8(4-1)5-3-7-10-9/h8-10H,1-7H2/p+1/t8-,9-/m0/s1

2051-28-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Decahydroquinoline

1.2 Other means of identification

Product number -
Other names decahydro-quinolin

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:2051-28-7 SDS

2051-28-7Relevant articles and documents

PRODUCTION METHOD OF CYCLIC COMPOUND

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Paragraph 0057; 0059; 0062-0063, (2021/05/05)

PROBLEM TO BE SOLVED: To provide an industrially simple production method of a cyclic compound. SOLUTION: A production method of a cyclic compound includes a step to obtain a reduced form (B) by reducing an unsaturated bond in a ring structure of an aromatic compound (A) by means of catalytic hydrogenation of the aromatic compound (A) or its salt using palladium carbon as a catalyst under a normal pressure, in which the aromatic compound (A) has one or more ring structures selected from a group consisting of a five membered-ring, a six membered-ring, and a condensed ring of the five membered-ring or the six membered-ring with another six membered-ring, a hetero atom can be included in the ring structure, and the aromatic compound (A) can have one or two side chains bonded to the ring structure and does not have any carbon-carbon triple bond in the side chain. SELECTED DRAWING: None COPYRIGHT: (C)2021,JPOandINPIT

A confined thermal transformation strategy to synthesize single atom catalysts supported on nitrogen-doped mesoporous carbon nanospheres for selective hydrogenation

Tian, Zhengbin,Wang, Guang-Hui,Wang, Wenquan,Zheng, Yan

, p. 25488 - 25494 (2021/12/07)

Carbon-supported single-atom catalysts (SACs) have brought considerable attention to heterogeneous catalysis, but they, however, often suffer from low activity due to the mass transfer limitation. Herein, we report a soft-templating method to synthesize core-shell mesostructured polymer nanospheres with metal nanoclusters (M-NCs, M = Pd, Pt) as the core, which can be easily converted into nitrogen-doped mesoporous carbon nanosphere (NMCS) supported SACs (M1/NMCS) after a confined thermal transformation process. Through this strategy, Pd1/NMCS and Pt1/NMCS are successfully prepared with rich porosity and high N content. The abundant N species in M1/NMCS can be employed as anchoring sites to capture and stabilize the single metal atoms. In addition, the mesoporous structure of M1/NMCS is beneficial for the mass transfer and the exposure of active sites. Benefiting from such a unique structure, the as-obtained Pd1/NMCS exhibits excellent activity, selectivity, and long-term stability in the selective hydrogenation of quinoline.

Aromatic compound hydrogenation and hydrodeoxygenation method and application thereof

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Paragraph 0094-0095; 0114-0122, (2021/05/29)

The invention belongs to the technical field of medicines, and discloses an aromatic compound hydrogenation and hydrodeoxygenation method under mild conditions and application of the method in hydrogenation and hydrodeoxygenation reactions of the aromatic compounds and related mixtures. Specifically, the method comprises the following steps: contacting the aromatic compound or a mixture containing the aromatic compound with a catalyst and hydrogen with proper pressure in a solvent under a proper temperature condition, and reacting the hydrogen, the solvent and the aromatic compound under the action of the catalyst to obtain a corresponding hydrogenation product or/and a hydrodeoxygenation product without an oxygen-containing substituent group. The invention also discloses specific implementation conditions of the method and an aromatic compound structure type applicable to the method. The hydrogenation and hydrodeoxygenation reaction method used in the invention has the advantages of mild reaction conditions, high hydrodeoxygenation efficiency, wide substrate applicability, convenient post-treatment, and good laboratory and industrial application prospects.

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