P9900
Perfluorodecalin
95%
동의어(들):
Octadecafluorodecahydronaphthalene (cis+trans), Perflunafene, Perfluorodecahydronaphthalene (cis+trans)
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모든 사진(1)
About This Item
실험식(Hill 표기법):
C10F18
CAS Number:
Molecular Weight:
462.08
Beilstein:
2067113
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
vapor density
17.5 (vs air)
Quality Level
분석
95%
refractive index
n20/D 1.3145 (lit.)
bp
142 °C (lit.)
mp
−10 °C (lit.)
density
1.908 g/mL at 25 °C (lit.)
SMILES string
FC1(F)C(F)(F)C(F)(F)C2(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C2(F)C1(F)F
InChI
1S/C10F18/c11-1-2(12,5(17,18)9(25,26)7(21,22)3(1,13)14)6(19,20)10(27,28)8(23,24)4(1,15)16
InChI key
UWEYRJFJVCLAGH-UHFFFAOYSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
Perfluorodecalin is a fluorous solvent generally used as a primary component of the fluorous biphasic system (FBS) or the fluorous multiphasic system (FMS) in synthetic chemistry. It is also used as an additive to increase oxygen solubility in fermentation media.
이미 열람한 고객
Palladium-Catalyzed Oxidation and Cyclization of Carbon-Carbon Triple Bonds in Fluorous Media Using Molecular Oxygen.
Wen Y, et al.
Synlett, 2011(07), 1023-1027 (2011)
Helen G Pennington et al.
PLoS pathogens, 15(3), e1007620-e1007620 (2019-03-12)
The biotrophic fungal pathogen Blumeria graminis causes the powdery mildew disease of cereals and grasses. We present the first crystal structure of a B. graminis effector of pathogenicity (CSEP0064/BEC1054), demonstrating it has a ribonuclease (RNase)-like fold. This effector is part
Three-component one-pot synthesis of pyrimidinone derivatives in fluorous media: Ytterbium bis (perfluorooctanesulfonyl) imide complex catalyzed Biginelli-type reaction.
Hong M and Cai C
Journal of Heterocyclic Chemistry, 46(6), 1430-1432 (2009)
Dilution-free analysis from picoliter droplets by nano-electrospray ionization mass spectrometry.
Ryan T Kelly et al.
Angewandte Chemie (International ed. in English), 48(37), 6832-6835 (2009-08-19)
Convenient electrophilic fluorination of functionalized aryl and heteroaryl magnesium reagents.
Yamada S, et al.
Angewandte Chemie (International Edition in English), 122(12), 2261-2264 (2010)
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