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21368-80-9

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21368-80-9 Usage

General Description

4-Ethynylphenyl ether, also known as 4-ethynylphenol or 4-ethynylphenyl, is an organic compound with the chemical formula C8H6O. It is a phenyl ether derivative that contains an ethynyl group, which is a triple-bonded carbon at position 4 of the phenyl ring. 4-Ethynylphenyl ether is often used as a building block in organic synthesis and can be utilized in the production of various pharmaceuticals, dyes, and organic compounds due to its unique reactivity and structure. It is a colorless to pale yellow liquid with a pungent odor and is considered to be a potential environmental contaminant. Its precise applications and uses may vary depending on the specific industry and research context in which it is employed.

Check Digit Verification of cas no

The CAS Registry Mumber 21368-80-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,3,6 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 21368-80:
(7*2)+(6*1)+(5*3)+(4*6)+(3*8)+(2*8)+(1*0)=99
99 % 10 = 9
So 21368-80-9 is a valid CAS Registry Number.

21368-80-9SDS

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 1-ethynyl-4-(4-ethynylphenoxy)benzene

1.2 Other means of identification

Product number -
Other names p,p'-diethynyldiphenylether

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:21368-80-9 SDS

21368-80-9Relevant articles and documents

Spatial extent of the singlet and triplet excitons in luminescent angular-shaped transition-metal diynes and polyynes comprising non-π-conjugated Group 16 main group elements

Poon, Suk-Yue,Wong, Wai-Yeung,Cheah, Kok-Wai,Shi, Jian-Xin

, p. 2550 - 2563 (2006)

A novel approach based on conjugation interruption has been developed and is presented for a series of luminescent and thermally stable chalcogen-bridged platinum(II) polyyne polymers trans-[{-Pt(PBu3)2C≡C- (C6H4/sub

Synthesis of ethynyl end-capped oligo-aryl ethers

Xu, Jinfeng,Lai, Guo-Qiao,Wang, Cheng-Yun,Shen, Yong-Jia

, p. 572 - 574 (2007/10/03)

A series of aryl ether oligomers end-capped with ethynyl groups have been synthesised via a three-step process, i.e. iodination of oligo-aryl ethers, nucleophilic substitution of the iodide group with 2-methyl-3-butyn-2-ol catalysed by Pd/Cu and subsequen

Synthesis of Arylacetylenes by the Sodium Hydride Catalyzed Cleavage of 4-Aryl-2-methyl-3-butyn-2-ols

Havens, Stephen J.,Hergenrother, Paul M.

, p. 1763 - 1765 (2007/10/02)

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