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202191-12-6

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202191-12-6 Usage

General Description

2-(4,5-Dihydro-2-oxazolyl)quinoline is a chemical compound that is 97% pure. It is a derivative of quinoline, a heterocyclic aromatic organic compound. 2-(4,5-Dihydro-2-oxazolyl)quinoline 97% contains a quinoline ring with a 2-oxazolyl group attached to it. The 97% purity indicates that the compound is highly pure and free from impurities, making it suitable for various research and industrial applications. This chemical may potentially have pharmaceutical, agrochemical, or material science applications, and its high purity makes it a valuable tool for further research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 202191-12-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,2,1,9 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 202191-12:
(8*2)+(7*0)+(6*2)+(5*1)+(4*9)+(3*1)+(2*1)+(1*2)=76
76 % 10 = 6
So 202191-12-6 is a valid CAS Registry Number.

202191-12-6 Well-known Company Product Price

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  • Aldrich

  • (713910)  2-(4,5-Dihydro-2-oxazolyl)quinoline  97%

  • 202191-12-6

  • 713910-500MG

  • 967.59CNY

  • Detail

202191-12-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-quinolin-2-yl-4,5-dihydro-1,3-oxazole

1.2 Other means of identification

Product number -
Other names 2-(quinoline-2-yl)-oxazoline

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:202191-12-6 SDS

202191-12-6Downstream Products

202191-12-6Relevant articles and documents

Concise Total Synthesis of (?)-Vermiculine through a Rhodium-Catalyzed C2-Symmetric Dimerization Strategy

Steib, Philip,Breit, Bernhard

, p. 3532 - 3535 (2019)

A short and efficient synthesis of the C2-symmetric antibiotic (?)-vermiculine by utilizing an enantioselective catalytic one-step dimerization methodology as key-step to construct the core structure is reported. The late-stage modifications feature a double metathesis homologation followed by a double Wacker-type oxidation. These key-steps allowed the synthesis of vermiculine in only seven steps, starting from commercially available building blocks.

Pyridine-oxazoline and quinoline-oxazoline ligated cobalt complexes: Synthesis, characterization, and 1,3-butadiene polymerization behaviors

Guo, Jun,Liu, Heng,Bi, Jifu,Zhang, Chunyu,Zhang, Hexin,Bai, Chenxi,Hu, Yanming,Zhang, Xuequan

, p. 305 - 312 (2015/08/06)

A series of cobalt complexes supported by pyridine-oxazoline (Pyox) and quinoline-oxazoline (Quox) were synthesized. Determined by single crystal X-ray crystallography, complexes 6a and 7c adopted distorted octahedron and trigonal bipyramid geometries, re

Catalyst-controlled Wacker-type oxidation of protected allylic amines

Michel, Brian W.,McCombs, Jessica R.,Winkler, Andrea,Sigman, Matthew S.

supporting information; experimental part, p. 7312 - 7315 (2010/11/05)

On the contrary: Utilizing the [Pd-(quinox)]-TBHP catalyst system, protected allylic amines were oxidized with high selectivity for the methyl ketone product. This is contrary to the results obtained by the substrate-controlled Tsuji-Wacker oxidation, which highlights the catalyst-controlled system presented here (see scheme). A variety of N-pro-tecting groups undergo selective oxidation with high ketone selectivity. TBHP = tert-butylhydroperoxide.

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