All Photos(3)
Synonym(s):
1-Ethynyl-2-methoxybenzene
Linear Formula:
HC≡CC6H4OCH3
CAS Number:
Molecular Weight:
132.16
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
form
liquid
refractive index
n20/D 1.5720 (lit.)
bp
197 °C (lit.)
density
1.022 g/mL at 25 °C (lit.)
SMILES string
COc1ccccc1C#C
InChI
1S/C9H8O/c1-3-8-6-4-5-7-9(8)10-2/h1,4-7H,2H3
InChI key
UFOVULIWACVAAC-UHFFFAOYSA-N
Related Categories
General description
2-Ethynylanisole is an acetylene derivative. It has been prepared by reacting 2-iodoanisole with trimethylsilylacetylene followed by the deprotection of trimethylsilyl group.
Application
2-Ethynylanisole may be used in the synthesis of 1,4-bis(2-methoxyphenyl)-2-methylbenzene.
WGK
WGK 3
Flash Point(F)
196.0 °F
Flash Point(C)
91.1 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Synthesis of Π-conjugated polymers via regioregular organometallic polymers 2. Transformation of titanacyclopentadiene-containing polymer into poly (p-phenylene) derivative.
Kino THN and Tomita I.
Applied Organometallic Chemistry, 24(8), 558-562 (2010)
T Iijima et al.
Chemical & pharmaceutical bulletin, 47(3), 398-404 (1999-04-23)
Synthesis and biological evaluation of the first dicarba-closo-dodecaborane (carborane) derivatives of retinoids are described. Their retinoidal activity were examined in terms of the differentiation-inducing ability toward human promyelocytic leukemia HL-60 cells. High retinoidal activity (agonist or antagonist for retinoic acid
The acid-catalysed synthesis of 7-azaindoles from 3-alkynyl-2-aminopyridines and their antimicrobial activity.
Leboho TC, et al.
Organic & Biomolecular Chemistry, 12(2), 307-315 (2014)
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