520039
2-Ethynylbenzyl alcohol
95%
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About This Item
Linear Formula:
HC≡CC6H4CH2OH
CAS Number:
Molecular Weight:
132.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Product Name
2-Ethynylbenzyl alcohol, 95%
InChI key
ZKCWIJQOZHADEM-UHFFFAOYSA-N
SMILES string
OCc1ccccc1C#C
InChI
1S/C9H8O/c1-2-8-5-3-4-6-9(8)7-10/h1,3-6,10H,7H2
assay
95%
form
solid
mp
66-70 °C (lit.)
functional group
hydroxyl
Quality Level
Related Categories
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Resp. Sens. 1
Storage Class
11 - Combustible Solids
wgk
WGK 2
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Cyclization reactions of 2-alkynylbenzyl alcohol and 2-alkynylbenzylamine derivatives promoted by tetrabutylammonium fluoride.
Hiroya K, et al.
Tetrahedron, 57(48), 9697-9710 (2001)
Preparation, Structural and Spectral Properties of Poly (2-ethynylbenzyl alcohol).
Lee WC, et al.
Mol. Cryst. Liq. Cryst., 513(1), 196-204 (2009)
Xueqing Wang et al.
The Journal of organic chemistry, 63(21), 7357-7363 (2001-10-24)
An attempt to trap radical intermediates during the monoamine oxidase (MAO) catalyzed oxidation of amines by intramolecular cyclization with an activated alkene that is built into the substrate was unsuccessful. (E)-2-(Iodoethenyl)benzylamine (3a) was shown to be a reversible inhibitor of
Synthesis of 1-(Alkoxycarbonyl) methylene-1, 3-dihydroisobenzofurans and 4-(Alkoxycarbonyl) benzo [c] pyrans by Palladium-Catalysed Oxidative Carbonylation of 2-Alkynylbenzyl Alcohols, 2-Alkynylbenzaldehydes and 2-Alkynylphenyl Ketones.
Bacchi A, et al.
European Journal of Organic Chemistry, 3, 574-585 (2004)
Subhasish Tapadar et al.
Bioorganic & medicinal chemistry, 23(24), 7543-7564 (2015-11-21)
Inhibition of the enzymatic activity of histone deacetylase (HDAC) is a promising therapeutic strategy for cancer treatment and several distinct small molecule histone deacetylase inhibitors (HDACi) have been reported. We have previously identified a new class of non-peptide macrocyclic HDACi
Articles
Alkynes' versatility enables reactions like addition, metathesis, hydroboration, cleavage, coupling, and cycloadditions in synthetic chemistry.
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