추천 제품
Quality Level
분석
97%
형태
liquid
refractive index
n20/D 1.498 (lit.)
bp
93-94 °C/113 mmHg (lit.)
density
1.438 g/mL at 25 °C (lit.)
작용기
alkyl halide
bromo
SMILES string
CCC#CCBr
InChI
1S/C5H7Br/c1-2-3-4-5-6/h2,5H2,1H3
InChI key
VDHGRVFJBGRHMD-UHFFFAOYSA-N
일반 설명
1-Bromo-2-pentyne is an halogenated hydrocarbon.
애플리케이션
1-Bromo-2-pentyne may be employed for the following syntheses:
- stereochemically restricted lactone-type analogs of jasmonic acids, 5-oxa-7-epi-jasmonic acid and 5-oxa-jasmonic acid
- 4,7-decadienal, 4,7-tridecadienal, 5,8-tetradecadienal and 6,9-dodecadienal (all-cis)
- 5-ethyl-4-methylene-6-phenyl-3a,4,7,7a-tetrahydroisobenzofuran-1,3-dione
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point (°F)
105.8 °F - closed cup
Flash Point (°C)
41 °C - closed cup
이미 열람한 고객
Synthesis of Cyclic Compounds Having exo-Methylene Groups through the Diels-Alder Reactions of Vinyl Allenes Obtained from Propargyl Bromide and Indium.
Bull. Korean Chem. Soc., 29(2), 487-487 (2008)
Synthesis of some aliphatic dienals.
Rec. Trav. Chim., 88(2), 177-184 (1969)
Bioscience, biotechnology, and biochemistry, 64(9), 1988-1992 (2000-10-31)
5-Oxa-7-epi-jasmonic acid and 5-oxa-jasmonic acid, which are stereochemically restricted lactone-type analogues of jasmonic acids, were synthesized via three-component coupling of 2(5H)-furanone, tert-butyl acetate and 1-bromo-2-pentyne. After acidic deprotection of the tert-butyl esters, the (Z)-olefin was introduced by catalytic partial reduction
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