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B0383

Sigma-Aldrich

Benzil

Synonym(e):

Dibenzoyl, Diphenylethandion

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About This Item

Lineare Formel:
C6H5COCOC6H5
CAS-Nummer:
134-81-6
Molekulargewicht:
210.23
Beilstein:
608047
EG-Nummer:
205-157-0
MDL-Nummer:
MFCD00003080
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24891516

Dampfdruck

1 mmHg ( 128.4 °C)

mp (Schmelzpunkt)

94-95 °C (lit.)

SMILES String

O=C(c1ccccc1)C(=O)c2ccccc2

InChI

1S/C14H10O2/c15-13(11-7-3-1-4-8-11)14(16)12-9-5-2-6-10-12/h1-10H

InChIKey

WURBFLDFSFBTLW-UHFFFAOYSA-N

Angaben zum Gen

human ... ACHE(43) , BCHE(590) , CES1(1066)

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Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H315,H319

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

356.0 °F - closed cup

Flammpunkt (°C)

180 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

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meso-Hydrobenzoin 99%

Sigma-Aldrich

294535

meso-Hydrobenzoin

Benzoin purified by sublimation, ≥99.5%

Sigma-Aldrich

399396

Benzoin

Hydrobenzoin

Sigma-Aldrich

301426

Hydrobenzoin

Craig E Wheelock et al.
Bioorganic & medicinal chemistry, 16(4), 2114-2130 (2007-11-21)
Carboxylesterases metabolize numerous exogenous and endogenous ester-containing compounds including the chemotherapeutic agent CPT-11, anti-influenza viral agent oseltamivir, and many agrochemicals. Trifluoromethyl ketone (TFK)-containing compounds with a sulfur atom beta to the ketone moiety are some of the most potent carboxylesterase
Elizabeth I Parkinson et al.
Bioorganic & medicinal chemistry, 19(15), 4635-4643 (2011-07-08)
Carboxylesterases (CE) are ubiquitous enzymes found in both human and animal tissues and are responsible for the metabolism of xenobiotics. This includes numerous natural products, as well as a many clinically used drugs. Hence, the activity of these agents is
Latorya D Hicks et al.
Bioorganic & medicinal chemistry, 15(11), 3801-3817 (2007-04-03)
We have synthesized and assessed the ability of symmetrical fluorobenzoins and fluorobenzils to inhibit mammalian carboxylesterases (CE). The majority of the latter were excellent inhibitors of CEs however unexpectedly, the fluorobenzoins were very good enzyme inhibitors. Positive correlations were seen
Janice L Hyatt et al.
Journal of medicinal chemistry, 48(17), 5543-5550 (2005-08-19)
Benzil has been identified as a potent selective inhibitor of carboxylesterases (CEs). Essential components of the molecule required for inhibitory activity include the dione moiety and the benzene rings, and substitution within the rings affords increased selectivity toward CEs from
Toshiyuki Harada et al.
Bioorganic & medicinal chemistry, 17(1), 149-164 (2008-12-09)
Carboxylesterases are enzymes that hydrolyze a broad suite of endogenous and exogenous ester-containing compounds to the corresponding alcohol and carboxylic acid. These enzymes metabolize a number of therapeutics including the anti-tumor agent CPT-11, the anti-viral drug oseltamivir, and the anti-thrombogenic
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