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597430

Sigma-Aldrich

4-Ethynylbenzaldehyde

97%

Synonym(s):

4-Formylphenylacetylene, p-Ethynylbenzaldehyde

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About This Item

Linear Formula:
HC≡CC6H4CHO
CAS Number:
Molecular Weight:
130.14
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

solid

mp

89-93 °C (lit.)

functional group

aldehyde

SMILES string

O=Cc1ccc(cc1)C#C

InChI

1S/C9H6O/c1-2-8-3-5-9(7-10)6-4-8/h1,3-7H

InChI key

BGMHQBQFJYJLBP-UHFFFAOYSA-N

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Yuki Maeda et al.
Journal of chromatography. A, 1355, 206-210 (2014-07-09)
A novel pre-column fluorescence derivatization method for chromatographic analysis of azide compounds was developed based on the Huisgen reaction, which is a specific cycloaddition reaction between an alkyne and an azide. We designed and synthesized a fluorescent alkyne, 2-(4-ethynylphenyl)-4,5-diphenyl-1H-imidazole (DIB-ET)
Gaulthier Rydzek et al.
ACS nano, 8(5), 5240-5248 (2014-04-18)
Simple preparation methods of chemically versatile and highly functionalizable surfaces remain rare and present a challenging research objective. Here, we demonstrate a simultaneous electropolymerization and electro-click functionalization process (SEEC) for one-pot self-construction of aniline- and naphthalene-based functional polymer films where

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