P8126
Phenylpyruvic acid
Sinonimo/i:
2-Oxo-3-phenylpropanoic acid, 2-Oxo-3-phenylpropionic acid
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About This Item
Formula condensata:
C6H5CH2COCOOH
Numero CAS:
Peso molecolare:
164.16
Beilstein:
2207312
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
Prezzi e disponibilità al momento non sono disponibili
Prodotti consigliati
Punto di fusione
150-154 °C (lit.)
Temperatura di conservazione
−20°C
Stringa SMILE
OC(=O)C(=O)Cc1ccccc1
InChI
1S/C9H8O3/c10-8(9(11)12)6-7-4-2-1-3-5-7/h1-5H,6H2,(H,11,12)
BTNMPGBKDVTSJY-UHFFFAOYSA-N
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Avvertenza
May decompose in storage, especially if not dry.
Codice della classe di stoccaggio
13 - Non Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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Faqing Tang et al.
Clinical biochemistry, 44(8-9), 711-718 (2011-03-16)
To search for markers of nasopharyngeal carcinoma (NPC) for diagnosis. Using gas chromatography and mass spectrometry, we evaluated 51 serum metabolites in 49 NPC, 37 throat cancer patients and 40 healthy controls. High metabolites were selected and confirmed in NPC
Sumit Chakraborty et al.
Biochemistry, 47(12), 3800-3809 (2008-03-05)
Direct spectroscopic observation of thiamin diphosphate-bound intermediates was achieved on the enzyme benzaldehyde lyase, which carries out reversible and highly enantiospecific conversion of ( R)-benzoin to benzaldehyde. The key enamine intermediate could be observed at lambda max 393 nm in
Nucleophile selectivity of chorismate-utilizing enzymes.
Olivier Kerbarh et al.
Chembiochem : a European journal of chemical biology, 8(6), 622-624 (2007-03-06)
Tapan Kanti Paine et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 13(21), 6073-6081 (2007-05-01)
Iron(II)-phenylpyruvate complexes of tetradentate tris(6-methyl-2-pyridylmethyl)amine (6-Me3-TPA) and tridentate benzyl bis(2-quinolinylmethyl)amine (Bn-BQA) were prepared to gain insight into C-C bond cleavage catalyzed by dioxygenase enzymes. The complexes we have prepared and characterized are [Fe(6-Me3-tpa)(prv)][BPh4] (1), [Fe2(6-Me3-tpa)2(pp)][(BPh4)2] (2), and [Fe2(6-Me3-tpa)2(2'-NO2-pp)][(BPh4)2] (3), [Fe(6-Me3-tpa)(pp-Me)][BPh4]
Gerrit J Poelarends et al.
Biochemistry, 46(33), 9596-9604 (2007-07-31)
The enzymatic conversion of cis- or trans-3-chloroacrylic acid to malonate semialdehyde is a key step in the bacterial degradation of the nematocide 1,3-dichloropropene. Two mechanisms have been proposed for the isomer-specific hydrolytic dehalogenases, cis- and trans-3-chloroacrylic acid dehalogenase (cis-CaaD and
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