추천 제품
분석
99%
형태
liquid
refractive index
n20/D 1.564 (lit.)
bp
185 °C (lit.)
density
0.928 g/mL at 25 °C (lit.)
저장 온도
2-8°C
SMILES string
CC#Cc1ccccc1
InChI
1S/C9H8/c1-2-6-9-7-4-3-5-8-9/h3-5,7-8H,1H3
InChI key
GHUURDQYRGVEHX-UHFFFAOYSA-N
일반 설명
Co-catalyzed reaction between cyclopentene and 1-phenyl-1-propyne has been reported. Bonding properties of 1-phenyl-1-propyne on Cu(111) at 100K have been studied using temperature-programmed desorption and X-ray, ultraviolet and two-photon photoemission spectroscopies. 1-Phenyl-1-propyne is an inhibitor of dopamine beta-hydroxylase. Polymerization of 1-phenyl-1-propyne by TaCl5 and NbCl5 has been reported.
1-Phenyl-1-propyne serves as a starting material for various chemical reactions, such as addition reactions and polymerization.
1-Phenyl-1-propyne serves as a starting material for various chemical reactions, such as addition reactions and polymerization.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
143.6 °F - closed cup
Flash Point (°C)
62 °C - closed cup
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Langmuir : the ACS journal of surfaces and colloids, 23(24), 12185-12191 (2007-10-31)
The bonding properties of 1-phenyl-1-propyne (PP, C6H5CCCH3) on Cu(111) at 100 K have been studied using temperature-programmed desorption (TPD), and X-ray, ultraviolet, and two-photon photoemission spectroscopies (XPS, UPS, and 2PPE). In TPD, there is no evidence for dissociation. Multilayer desorption
(Arylimido)niobium(V)?Alkylidenes, Nb(CHSiMe3)(NAr)[OC(CF3)3](PMe3)2, That Enable to Proceed Living Metathesis Polymerization of Internal Alkynes
Macromolecules, 53(13), 5266-5279 (2020)
Journal of the American Chemical Society, 136(16), 5832-5835 (2014-04-12)
Here we report a general method for the measurement of (13)C kinetic isotope effects at natural abundance for reactions that yield two or more products concurrently. We use, as an example, a recently reported Co-catalyzed reaction between cyclopentene and 1-phenyl-1-propyne.
Effect of organometallic cocatalysts on the polymerization of 1-phenyl-1-propyne by tantalum pentachloride (TaCl5) and niobium pentachloride (NbCl5).
Macromolecules, 18(11), 2109-2113 (1985)
The Journal of biological chemistry, 259(24), 15017-15020 (1984-12-25)
The catalytic action of dopamine beta-hydroxylase on 1-phenyl-1-propyne results in concomitant loss of enzyme activity. At pH 5.5 and 25 degrees C, 1-phenyl-1-propyne inactivates dopamine beta-hydroxylase in a mechanism-based fashion. The inactivation rate is first-order, follows saturation kinetics, and is
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