Skip to Content
Merck
CN

557331

3-Ethynyl-α,α,α-trifluorotoluene

97%

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
HC≡CC6H4CF3
CAS Number:
Molecular Weight:
170.13
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI

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

SMILES string

FC(F)(F)c1cccc(c1)C#C

InChI key

PAHXLHWOHJTWRU-UHFFFAOYSA-N

assay

97%

refractive index

n20/D 1.464 (lit.)

bp

146 °C (lit.)

density

1.178 g/mL at 25 °C (lit.)

functional group

fluoro

Application

3-Ethynyl-α,α,α-trifluorotoluene may be used to synthesize:
  • 1-thioacetyl-4[3-trifluoromethyl-1-(ethynyl)phenyl]benzene
  • 4-{[4-(3-(trifluoromethyl)phenyl)-1H-1,2,3-triazol-1-yl]methyl}benzoic acid
  • 4-{4-[3-(trifluoromethyl)phenyl]-1H-1,2,3-triazol-1-yl}benzoic acid

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

69.8 °F - closed cup

flash_point_c

21 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
This item has

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

Matthias Wrobel et al.
Beilstein journal of organic chemistry, 8, 1027-1036 (2012-09-29)
A series of substituted diaryltriazoles was prepared by a solid-phase-synthesis protocol using a modified Wang resin. The copper(I)- or ruthenium(II)-catalyzed 1,3-cycloaddition on the polymer bead allowed a rapid synthesis of the target compounds in a parallel fashion with in many
Synthesis, structural analysis, and self-assembly of phenylene ethynylene oligomers and their F, CF3, and CH3 substituted derivatives.
Percec S, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 42(3), 541-550 (2004)

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