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Quinoline, 2-(1-methylethenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15825-90-8

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15825-90-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15825-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,2 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15825-90:
(7*1)+(6*5)+(5*8)+(4*2)+(3*5)+(2*9)+(1*0)=118
118 % 10 = 8
So 15825-90-8 is a valid CAS Registry Number.

15825-90-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-prop-1-en-2-ylquinoline

1.2 Other means of identification

Product number -
Other names Quinoline,2-(1-methylethenyl)

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:15825-90-8 SDS

15825-90-8Relevant academic research and scientific papers

Facile catalyst-free synthesis of 2-vinylquinolines via a direct deamination reaction occurring during Mannich synthesis

Xiao, Jichao,Huang, Ye,Song, Zilan,Feng, Wenhua

, p. 99095 - 99098 (2015)

A facile catalyst-free method for the synthesis of 2-vinylquinolines via a direct deamination reaction during Mannich synthesis has been developed. Instantaneous hydrogen transfer via a six-membered ring intermediate is proposed as a key step for the direct deamination reaction. This reaction strategy tolerates a broad substrate scope and provides a highly efficient way to synthesize 2-vinylquinolines with adequate yields.

A SIMPLE REGIOSELECTIVE PREPARATION OF 2- OR 3-SUBSTITUTED QUINOLINE DERIVATIVES VIA DIALKYLQUINOLYLBORANES

Ishikura, Minoru,Oda, Izumi,Terashima, Masanao

, p. 2375 - 2386 (2007/10/02)

Various quinoline derivatives possessing a substituent at the 2- or 3-position were prepared by the reaction of dialkylquinolylboranes and organic bromides in the presence of a palladium catalyst.

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