추천 제품
Grade
technical grade
Quality Level
분석
90%
형태
liquid
refractive index
n20/D 1.467 (lit.)
bp
97-99 °C/20 mmHg (lit.)
density
1.13 g/mL at 25 °C (lit.)
작용기
ester
SMILES string
CC1=CCOC1=O
InChI
1S/C5H6O2/c1-4-2-3-7-5(4)6/h2H,3H2,1H3
InChI key
VGHBEMPMIVEGJP-UHFFFAOYSA-N
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일반 설명
3-Methyl-2(5H)-furanone (3-Methylfuran-2(5H)-one) has been synthesized in highest yield (77%) by employing α-methyl-γ- butyrolactone as starting reagent.
3-Methyl-2(5H)-furanone, a five membered conjugated lactone, is a volatile compound. Its synthesis has been reported. It is reported to be one of the predominant constituent of the flavor of pandan leaves. It is also found in Thai soy sauce, Arabica roasted coffee samples from Brazil, bio-oil from pine wood sawdust.
애플리케이션
3-Methyl-2(5H)-furanone is the suitable model compound used to investigate the fragmentation mechanism of five membered lactones by electrospray ionisation tandem mass spectrometry and also to study the airway irritation of isoprene, isoprene/ozone, and isoprene/ozone/nitrogen dioxide mixture.
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)
200.1 °F - closed cup
Flash Point (°C)
93.4 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
The fragmentation mechanism of five-membered lactones by electrospray ionisation tandem mass spectrometry.
International Journal of Mass Spectrometry, 232(3), 271-276 (2004)
A New Expedient Synthesis of 3-Methyl-2 (5H)-furanone, the Common Substructure in Strigolactones, and Its Proposed Biosynthesis.
Synthesis, 19, 3271-3273 (2010)
Supercritical carbon dioxide extraction of 2-acetyl-1-pyrroline and volatile components from pandan leaves.
Flavour and Fragrance Journal, 19(3), 251-259 (2004)
An efficient and short synthesis of 3-methyl-2 (5H)-furanone, a synthon for strigol analogues.
Synthetic Communications, 22(5), 783-786 (1992)
A Useful Synthesis of 3-Methyl-2 (5H)-Furanone.
Synthetic Communications, 21(8-9), 1097-1104 (1991)
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