추천 제품
vapor pressure
186 mmHg ( 37.7 °C)
분석
99%
형태
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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애플리케이션
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.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
6.8 °F - closed cup
Flash Point (°C)
-14 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
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
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
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
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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