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306894

Sigma-Aldrich

3-Hexyne

99%

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About This Item

Fórmula lineal:
C2H5C≡CC2H5
Número de CAS:
928-49-4
Peso molecular:
82.14
Beilstein/REAXYS Number:
1731158
EC Number:
213-173-4
MDL number:
MFCD00009381
UNSPSC Code:
12352100
PubChem Substance ID:
24858544
NACRES:
NA.22

vapor pressure

186 mmHg ( 37.7 °C)

assay

99%

form

liquid

refractive index

n20/D 1.411 (lit.)

bp

81-82 °C (lit.)

density

0.723 g/mL at 25 °C (lit.)

SMILES string

CCC#CCC

InChI

1S/C6H10/c1-3-5-6-4-2/h3-4H2,1-2H3

InChI key

DQQNMIPXXNPGCV-UHFFFAOYSA-N

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Application

3-Hexyne was used in the synthesis of fused hetero-hydropyridyl ligands bonded to the {Ru(p-cymene)} organometallic moiety by reacting with ruthenacycles. It was also used in the preparation of [4+2] cycloaddition product by reacting with borole.

signalword

Danger

Hazard Classifications

Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

6.8 °F - closed cup

flash_point_c

-14 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Luciano Cuesta et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(47), 15178-15189 (2012-09-29)
Novel cycloruthenated complexes 2 a-c, 4 a-c, and 6 a, b based on heteroaromatic cores have been synthesized by reaction of a series of heterocycle-based imines with [{RuCl(η(6)-p-cymene)}(2)(μ-Cl)(2)] and Cu(OAc)(2). This approach has proved efficient for the cyclometalation of thiophene, benzothiophene, furan, benzofuran, pyrrole
Fang Ge et al.
Journal of the American Chemical Society, 136(1), 68-71 (2013-12-21)
Bis(trimethylsilylethynyl)diphenylaminoborane was reacted with the strong Lewis acid B(C6F5)3 at ambient temperature to give the borole 9 admixed with a small amount of its thermal follow-up product 12. Compound 9 was subsequently stabilized by adduct formation with pyridine (10). Treatment
He Nan et al.
Journal of chromatography. A, 1523, 316-320 (2017-06-26)
Silver ion or argentation chromatography utilizes stationary phases containing silver ions for the separation of unsaturated compounds. In this study, a mixed-ligand silver-based ionic liquid (IL) was evaluated for the first time as a gas chromatographic (GC) stationary phase for
Davide Albani et al.
Nature communications, 9(1), 2634-2634 (2018-07-08)
Ensemble control has been intensively pursued for decades to identify sustainable alternatives to the Lindlar catalyst (PdPb/CaCO3) applied for the partial hydrogenation of alkynes in industrial organic synthesis. Although the geometric and electronic requirements are known, a literature survey illustrates

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