196746
2,3,4,5,6-Pentafluorobenzyl alcohol
98%
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About This Item
Formula condensata:
C6F5CH2OH
Numero CAS:
Peso molecolare:
198.09
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
98%
Stato
solid
P. ebollizione
114-115 °C/60 mmHg (lit.)
Punto di fusione
37-38 °C (lit.)
Stringa SMILE
OCc1c(F)c(F)c(F)c(F)c1F
InChI
1S/C7H3F5O/c8-3-2(1-13)4(9)6(11)7(12)5(3)10/h13H,1H2
PGJYYCIOYBZTPU-UHFFFAOYSA-N
Descrizione generale
Structures of complex of horse liver alchohol dehydrogenase enzyme with 2,3,4,5,6-pentafluorobenzyl alcohol has been investigated by X-ray crystallography.
Applicazioni
2,3,4,5,6-Pentafluorobenzyl alcohol was used in the synthesis of pentafluorobenzyloxy substituted metal-free phthalocyanine.
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Acute Tox. 4 Oral
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
190.4 °F - closed cup
Punto d’infiammabilità (°C)
88 °C - closed cup
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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Structures of horse liver alcohol dehydrogenase complexed with NAD+ and substituted benzyl alcohols.
S Ramaswamy et al.
Biochemistry, 33(17), 5230-5237 (1994-05-03)
Structures of the enzyme complexed with NAD+ and 2,3,4,5,6-pentafluorobenzyl alcohol were determined by X-ray crystallography at a resolution of 2.1 A and to a refinement R value of 18.3% for a monoclinic (P2(1)) form and to 2.4 A and an
V G Voinov et al.
Analytical chemistry, 76(10), 2951-2957 (2004-05-18)
A prototype gas chromatograph (GC) electron monochromator (EM) reflectron time-of-flight (TOF) mass spectrometer has been constructed and demonstrated to simultaneously record four-dimensional resonant electron capture (REC) mass spectra (m/z, ion-intensity, electron-energy, and retention time) of electron-capturing compounds in real time.
C Oman
Environmental science & technology, 35(1), 232-239 (2001-05-16)
Emissions of organic compounds from landfills depend on the fate of the compounds inside the landfills. This field study was used to investigate the fate in landfills of organic compounds having different physical, chemical, and biological characteristics. For this purpose
Jon K Rubach et al.
Biochemistry, 41(52), 15770-15779 (2002-12-27)
The relationship between substrate mobility and catalysis was studied with wild-type and Phe93Ala (F93A) horse liver alcohol dehydrogenase (ADH). Wild-type ADH binds 2,3,4,5,6-pentafluorobenzyl alcohol in one position as shown by X-ray results, and (19)F NMR shows five resonances for the
Novel phthalocyanines with pentafluorobenzyloxy-substituents.
Selcukoglu M and Hamuryudan E.
Dyes and Pigments, 74(1), 17-20 (2007)
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