467227
2-Ethynylanisole
97%
Synonym(s):
1-Ethynyl-2-methoxybenzene
Sign Into View Organizational & Contract Pricing
All Photos(3)
About This Item
Linear Formula:
HC≡CC6H4OCH3
CAS Number:
Molecular Weight:
132.16
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
196.0 °F - closed cup
Flash Point(C)
91.1 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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)
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
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