T7392
D-(−)-Threose
≥60%, syrup
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关于此项目
经验公式（希尔记法）:
C4H8O4
化学文摘社编号:
分子量:
120.10
EC Number:
202-418-0
UNSPSC Code:
12352201
PubChem Substance ID:
Beilstein/REAXYS Number:
1721696
MDL number:
InChI key
FMAORJIQYMIRHF-URORKIPUSA-N
InChI
1S/C4H8O4/c5-2-1-8-4(7)3(2)6/h2-7H,1H2/t2-,3+,4?/m0/s1
SMILES string
O[C@H]1COC(O)[C@@H]1O
form
syrup
optical activity
[α]20/D -16.4 to -9.8 °, c = 2% (w/v) in water
concentration
≥60%
storage temp.
2-8°C
Quality Level
存储类别
12 - Non Combustible Liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
法规信息
新产品
此项目有
Allen Horhota et al.
Journal of the American Chemical Society, 127(20), 7427-7434 (2005-05-19)
alpha-l-Threofuranosyl nucleoside triphosphates (tNTPs) are tetrafuranose nucleoside derivatives and potential progenitors of present-day beta-d-2'-deoxyribofuranosyl nucleoside triphosphates (dNTPs). Therminator DNA polymerase, a variant of the 9 degrees N DNA polymerase, is an efficient DNA-directed threosyl nucleic acid (TNA) polymerase. Here we
Jussi Kinnunen et al.
Journal of biomedical optics, 17(9), 97003-97003 (2012-09-15)
Extensive collagen cross-linking affects the mechanical competence of articular cartilage: it can make the cartilage stiffer and more brittle. The concentrations of the best known cross-links, pyridinoline and pentosidine, can be accurately determined by destructive high-performance liquid chromatography (HPLC). We
Benjamin D Heuberger et al.
Organic letters, 8(25), 5809-5811 (2006-12-01)
Cytosine TNA promotes nonenzymatic, template-directed oligomerization of complementary activated rGMP, leading to selective and efficient formation of RNA products. This process models "genetic takeover" of a pre-RNA by RNA. [reaction: see text]
Zhenyu Dai et al.
Archives of biochemistry and biophysics, 463(1), 78-88 (2007-05-01)
We isolated a novel acid-labile yellow chromophore from the incubation of lysine, histidine and d-threose and identified its chemical structure by one and two-dimensional NMR spectroscopy combined with LC-tandem mass spectrometry. This new cross-link exhibits a UV absorbance maximum at
María Ruiz et al.
The Journal of organic chemistry, 73(6), 2240-2255 (2008-02-28)
A general strategy for the synthesis of 1-deoxy-azasugars from a chiral glycine equivalent and 4-carbon building blocks is described. Diastereoselective aldol additions of metalated bislactim ethers to matched and mismatched erythrose or threose acetonides and intramolecular N-alkylation (by reductive amination
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