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520039

Sigma-Aldrich

2-乙炔苯甲醇

95%

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About This Item

線性公式:
HC≡CC6H4CH2OH
CAS號碼:
10602-08-1
分子量：:
132.16
MDL號碼:
MFCD06200681
分類程式碼代碼:
12352100
PubChem物質ID:
24874088
NACRES:
NA.22

化驗

95%

形狀

solid

mp

66-70 °C (lit.)

官能基

hydroxyl

SMILES 字串

OCc1ccccc1C#C

InChI

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

InChI 密鑰

ZKCWIJQOZHADEM-UHFFFAOYSA-N

相關類別

象形圖

Health hazardExclamation mark
GHS08,GHS07

訊號詞

Danger

危險聲明

H302,H319,H334

危險分類

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 2

個人防護裝備

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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分析證明 (COA)

Lot/Batch Number
BGBC5434
BGBC1998
MKBJ3943V
MKBH3595V
MKAA4445

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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
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)
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
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文章

Functionalized Alkynes

Alkynes contain a highly versatile functional group that may be utilized for numerous reactions such as electrophilic additions of hydrogen, halogens, hydrogen halides, or water; metathesis; hydroboration; oxidative cleavage; C–C coupling; and cycloadditions

Functionalized Alkynes

Alkynes contain a highly versatile functional group that may be utilized for numerous reactions such as electrophilic additions of hydrogen, halogens, hydrogen halides, or water; metathesis; hydroboration; oxidative cleavage; C–C coupling; and cycloadditions

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