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10174-55-7

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10174-55-7 Usage

Type of compound

Derivative of quinoline, a heterocyclic aromatic compound

Common use

Building block in the synthesis of pharmaceutical and agrochemical products

Pharmacological properties

Anti-inflammatory and anti-microbial activities

Potential applications

Design and development of new materials

Examples of new materials

Fluorescent dyes and organic light-emitting diodes

Role in fields

Chemistry and biotechnology

Benefits

Diverse applications and potential for further research and development

Check Digit Verification of cas no

The CAS Registry Mumber 10174-55-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,7 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10174-55:
(7*1)+(6*0)+(5*1)+(4*7)+(3*4)+(2*5)+(1*5)=67
67 % 10 = 7
So 10174-55-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H11NO/c1-9(13)12-8-4-6-10-5-2-3-7-11(10)12/h2-7H,8H2,1H3

10174-55-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2H-quinolin-1-yl)ethanone

1.2 Other means of identification

Product number -
Other names Quinoline,1,2-dihydro-1-acetyl

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:10174-55-7 SDS

10174-55-7Relevant articles and documents

Synthesis of 1,2-Dihydroquinolines via Hydrazine-Catalyzed Ring-Closing Carbonyl-Olefin Metathesis

Zhang, Yunfei,Sim, Jae Hun,Macmillan, Samantha N.,Lambert, Tristan H.

, p. 6026 - 6030 (2020/08/05)

The synthesis of 1,2-dihydroquinolines by the hydrazine-catalyzed ring-closing carbonyl-olefin metathesis (RCCOM) of N-prenylated 2-aminobenzaldehydes is reported. Substrates with a variety of substitution patterns are shown. With an acid-labile protecting group on the nitrogen atom, in situ deprotection and autoxidation furnish quinoline. In comparison with related oxygen-containing substrates, the cycloaddition step of the catalytic cycle is shown to be slower, but the cycloreversion is found to be more facile.

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