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520039

Sigma-Aldrich

2-Ethynylbenzyl alcohol

95%

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About This Item

Linear Formula:
HC≡CC6H4CH2OH
CAS Number:
10602-08-1
Molecular Weight:
132.16
MDL number:
MFCD06200681
UNSPSC Code:
12352100
PubChem Substance ID:
24874088
NACRES:
NA.22
form:
solid
Assay:
95%

Assay

95%

form

solid

mp

66-70 °C (lit.)

functional group

hydroxyl

SMILES string

OCc1ccccc1C#C

InChI

1S/C9H8O/c1-2-8-5-3-4-6-9(8)7-10/h1,3-6,10H,7H2

InChI key

ZKCWIJQOZHADEM-UHFFFAOYSA-N

Related Categories

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Danger

Hazard Statements

H302,H319,H334

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Resp. Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

520039-VAR:
520039-BULK:
520039-5G:

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Certificates of Analysis (COA)

Lot/Batch Number
0000219795
0000236206
0000178687
BGBC5434
BGBC1998

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Preparation, Structural and Spectral Properties of Poly (2-ethynylbenzyl alcohol).
Lee WC, et al.
Mol. Cryst. Liq. Cryst., 513(1), 196-204 (2009)
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)
Cyclization reactions of 2-alkynylbenzyl alcohol and 2-alkynylbenzylamine derivatives promoted by tetrabutylammonium fluoride.
Hiroya K, et al.
Tetrahedron, 57(48), 9697-9710 (2001)
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
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
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Functionalized Alkynes

Alkynes' versatility enables reactions like addition, metathesis, hydroboration, cleavage, coupling, and cycloadditions in synthetic chemistry.

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