所有图片(3)
About This Item
线性分子式:
FCH2COCO2Na · H2O
CAS号:
分子量:
146.05
MDL號碼:
分類程式碼代碼:
12352106
PubChem物質ID:
NACRES:
NA.25
推荐产品
品質等級
化驗
≥98%
儲存溫度
−20°C
SMILES 字串
FCC(C([O-])=O)=O.O.[Na+]
InChI
1S/C3H3FO3.Na.H2O/c4-1-2(5)3(6)7;;/h1H2,(H,6,7);;1H2/q;+1;/p-1
InChI 密鑰
HDSZBLZMLDQKRW-UHFFFAOYSA-M
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
Cody W van Dijk et al.
The journal of physical chemistry. A, 116(16), 4082-4088 (2012-03-27)
The ground state rotational spectra of 2-fluoropyridine and 3-fluoropyridine have been investigated using both Fourier transform microwave (FTMW) and chirped pulse Fourier transform microwave (cp-FTMW) spectroscopies. In addition to the parent species, the spectra of the (13)C and (15)N singly
P Urban et al.
European journal of biochemistry, 144(2), 345-351 (1984-10-15)
It has been shown that reduced flavocytochrome b2 not only catalyzes reduction of bromopyruvate [P. Urban, P.M. Alliel and F. Lederer (1983) Eur. J. Biochem. 134, 275-281] but also transforms it into pyruvate in a reductive elimination process. The dehydrohalogenation
E B Borthwick et al.
The Biochemical journal, 305 ( Pt 2), 521-524 (1995-01-15)
Simplified procedures for assaying and purifying dihydrodipicolinate synthase (EC 4.2.1.52), the first enzyme of the lysine biosynthetic pathway, have been developed and electrospray ionization m.s. has been used to observe the imine intermediate with pyruvate and to investigate the reaction
Fluoropyruvate: a potent inhibitor of the bacterial and the mammalian pyruvate dehydrogenase complex.
H Bisswanger
Biochemical and biophysical research communications, 95(2), 513-519 (1980-07-31)
L G Korotchkina et al.
Archives of biochemistry and biophysics, 369(2), 277-287 (1999-09-16)
Pyruvate dehydrogenase (E1), a heterotetramer (alpha(2)beta(2)), is the first catalytic component of the mammalian pyruvate dehydrogenase complex (PDC). To investigate the roles of cysteine-62 of E1alpha (alphaC62) and tryptophan-135 of E1beta (betaW135) (identified previously as active site residues using chemical
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