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1613-32-7

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1613-32-7 Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 81, p. 4000, 1959 DOI: 10.1021/ja01524a045The Journal of Organic Chemistry, 40, p. 2288, 1975 DOI: 10.1021/jo00904a005

Check Digit Verification of cas no

The CAS Registry Mumber 1613-32-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,1 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1613-32:
(6*1)+(5*6)+(4*1)+(3*3)+(2*3)+(1*2)=57
57 % 10 = 7
So 1613-32-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H13N/c1-2-5-11-9-8-10-6-3-4-7-12(10)13-11/h3-4,6-9H,2,5H2,1H3

1613-32-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-propylquinoline

1.2 Other means of identification

Product number -
Other names 1-(2-quinolyl)propane

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:1613-32-7 SDS

1613-32-7Relevant articles and documents

-

Bergstrom

, p. 3027,3032, 3034 (1931)

-

-

Hata et al.

, p. 942,945 (1973)

-

Preparation of 3-hydroxyquinolines from direct oxidation of dihydroquinolinium salts

Ramanathan, Mani,Wan, Jing,Liu, Shiuh-Tzung

, p. 38166 - 38174 (2018)

A series of functionalized 3,4-dihydroquinolinium salts were prepared from the reaction of aryldiazonium salt with alkene in a nitrile solution. Further oxidation yielding either 3-hydroxyquinoline or quinoline products was investigated. A one-pot process from aryldiazonium salts, alkenes and nitriles leading to 3-hydroxyquinolines was also developed. Furthermore, an intramolecular trapping of an N-arylnitrilium ion with a vinyl group at the ortho position leading to 2-substituted quinolines was revealed.

Straightforward synthesis of 2-propylquinolines under multicomponent conditions in fluorinated alcohols

Venkateswarlu,Balaji,De, Kavita,Crousse, Benoit,Figadère, Bruno,Legros, Julien

, p. 94 - 98 (2013)

The synthesis of 2-propylquinolines, a family of antileishmanial agents, is reported. Among the pathways explored, the 3-component Povarov reaction between butyraldehyde, aromatic amines and ethyl vinyl ether in trifluoroethanol (TFE), followed by an oxidation, offers a convenient entry to 2-propylquinolines with various substituents on positions 5-8.

Method for preparing quinoline derivative

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Paragraph 0045-0046, (2020/02/17)

The invention relates to a method for preparing a quinoline derivative. The method comprises the following steps: by taking aromatic amine compounds and fatty alcohol as raw materials and oxygen-containing molybdenum disulfide as a catalyst, performing a reaction for 2-12 hours in an inert atmosphere or an oxygen-containing atmosphere at the temperature of 120-200 DEG C, after the reaction is finished, separating liquid phase components, performing concentration, and performing separation through a silica gel column, so as to obtain a substituted quinoline compound. The synthetic method may have important application in the aspect of quinoline compound synthesis.

Green synthesis of silver nanoparticles using green alga (Chlorella vulgaris) and its application for synthesis of quinolines derivatives

Mahajan, Akhil,Arya, Anju,Chundawat, Tejpal Singh

supporting information, p. 1926 - 1937 (2019/05/17)

Nanoparticles have been used century ago but have regained their importance in recent years being simple, ecofriendly, pollutant free, nontoxic, low-cost approach, and due good atom economy. In this report, we have demonstrated the synthesis of silver nanoparticles using green algae (Chlorella vulgaris) which in turn was used for synthesis of biologically important quinolines. Algal extract was prepared and treated with silver nitrate solution for the synthesis of silver nanoparticles. Synthesized nanoparticles were characterized with the help of analytical tools like UV, FTIR, X-ray, and SEM and used as a catalyst for the synthesis of quinolines.

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