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62484-52-0

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62484-52-0 Usage

General Description

4-ethynyl-quinoline is a chemical compound with the molecular formula C11H7N, consisting of a quinoline ring with an ethynyl group attached to the 4-position. It is a yellowish-brown crystalline solid that is mainly used as an intermediate in the synthesis of pharmaceuticals, dyes, and agrochemicals. 4-ETHYNYL-QUINOLINE is also employed in organic synthesis as a building block for various aromatic compounds. It is important to handle 4-ethynyl-quinoline with care, as it may be harmful if ingested or inhaled, and can cause skin and eye irritation upon contact. Its main applications include its use in the pharmaceutical industry and as a building block in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 62484-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,8 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62484-52:
(7*6)+(6*2)+(5*4)+(4*8)+(3*4)+(2*5)+(1*2)=130
130 % 10 = 0
So 62484-52-0 is a valid CAS Registry Number.

62484-52-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Ethynylquinoline

1.2 Other means of identification

Product number -
Other names 4-Ethinylchinolin

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:62484-52-0 SDS

62484-52-0Downstream Products

62484-52-0Relevant articles and documents

Mikhailov et al.

, (1977)

General and selective head-to-head dimerization of terminal alkynes proceeding via hydropalladation pathway

Jahier, Claire,Zatolochnaya, Olga V.,Zvyagintsev, Nickolay V.,Ananikov, Valentine P.,Gevorgyan, Vladimir

, p. 2846 - 2849 (2012/07/17)

A general highly regio- and stereoselective palladium-catalyzed head-to-head dimerization reaction of terminal acetylenes is presented. This methodology allows for the efficient synthesis of a variety of 1,4-enynes as single E stereoisomers. Computational studies reveal that this dimerization reaction proceeds via the hydropalladation pathway.

A Facile Synthesis of Ethynyl-Substituted Six-Membered N-Heteroaromatic Compounds

Sakamoto, Takao,Shiraiwa, Masafumi,Kondo, Yoshinori,Yamanaka, Hiroshi

, p. 312 - 314 (2007/10/02)

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