467227
2-Ethynylanisole
97%
Synonym(s):
1-Ethynyl-2-methoxybenzene
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About This Item
Linear Formula:
HC≡CC6H4OCH3
CAS Number:
Molecular Weight:
132.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
liquid
Quality Level
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
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
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Storage Class
12 - Non Combustible Liquids
flash_point_f
does not flash
flash_point_c
does not flash
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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
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)
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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 467227-5G | 04061832358093 |
| 467227-1G | 04061832358079 |