Skip to Content
Merck
All Photos(1)

Key Documents

Safety Information

556432

Sigma-Aldrich

4-Ethynyl-α,α,α-trifluorotoluene

97%

Synonym(s):

1-Ethynyl-4-(trifluoromethyl)benzen, 1-Ethynyl-4-(trifluoromethyl)benzene, 1-Trifluoromethyl-4-ethynylbenzene, 4-(Trifluoromethyl)phenylacetylene, 4-Ethynyl(trifluoromethyl)benzene, 4-Ethynyl-trifluorotoluene, 4-Trifluorophenylacetylene, [4-(Trifluoromethyl)phenyl]ethyne, p-(Trifluoromethyl)phenylacetylene

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
HC≡CC6H4CF3
CAS Number:
Molecular Weight:
170.13
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

refractive index

n20/D 1.4650 (lit.)

bp

78-80 °C/2 mmHg (lit.)

density

1.043 g/mL at 25 °C (lit.)

SMILES string

FC(F)(F)c1ccc(cc1)C#C

InChI

1S/C9H5F3/c1-2-7-3-5-8(6-4-7)9(10,11)12/h1,3-6H

InChI key

XTKBMZQCDBHHKY-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

4-Ethynyl-α,α,α-trifluorotoluene reacts with ethanol to afford the corresponding α,β-alkynyl ester. 4-Ethynyl-α,α,α-trifluorotoluene plays the role of a functionalized alkyne in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reaction on BrPP thin films.

Application

4-Ethynyl-α,α,α-trifluorotoluene may be used to synthesize the following:
  • 6,13-bis(4-trifluoromethylphenylethynyl)pentacene
  • 1,2-dialkynylimidazoles
  • trans-[Co(cyclam)(p-CCC6H4CF3)2]OTf complex (where cyclam - 1,4,8,11-tetraazacyclotetradecane; 4-ethynyl-α,α,α-trifluorotoluene - p-CCC6H4CF3; OTf- trifluoromethane sulfonate)
  • 3-spiroazetidinimine-2-oxindoles
Used to synthesize self-assembled monolayers (SAMs).

Pictograms

Flame

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

69.1 °F - closed cup

Flash Point(C)

20.6 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 1 petroleums
Hazardous rank II
Water insoluble liquid

JAN Code

556432-5G:
556432-BULK:
556432-VAR:


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

"A Copper-Catalyzed One-Pot, Three-Component Diastereoselective Synthesis of 3-Spiroazetidinimine-2-oxindoles and Their Synthetic Transformation into Fluorescent Conjugated Indolones"
Periyaraja S, et al.
European Journal of Organic Chemistry, 2014(5), 954-965 (2014)
"5H-Cyclopentapyrazines from 1, 2-Dialkynylimidazoles"
Kerwin.MS and Nadipuram A
Synlett, 2004(08), 1404-1408 (2004)
Rodney T Chen et al.
Langmuir : the ACS journal of surfaces and colloids, 26(5), 3388-3393 (2009-11-12)
A brominated plasma polymer (BrPP) thin film was fabricated on a variety of substrate surfaces (silicon wafers, glass, gold, and polymers) via the radio frequency glow discharge of 1-bromopropane. This BrPP thin film was highly adherent and stable and was
Journal of Polymer Science Part A: Polymer Chemistry, 42, 541-550 (2004)
Synthesis of α, β-Alkynyl Esters and Unsymmetrical Maleate Esters Catalyzed by Pd/C; An Efficient Phosphine-Free Catalytic System for Oxidative Alkoxycarbonylation of Terminal Alkynes.
Gadge ST and Bhanage BM.
Synlett, 24(8), 981-986 (2013)

Articles

The terminal alkyne functionality has a wide range of applications including most recently the synthesis of spiropyran substituted 2,3-dicyanopyrazines and (±)-asteriscanolide, as well as conversion to enamines using resin-bound 2° amines.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service