T7392
D-(−)-Threose
≥60%, syrup
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About This Item
Fórmula empírica (notación de Hill):
C4H8O4
Número de CAS:
Peso molecular:
120.10
Beilstein/REAXYS Number:
1721696
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
Productos recomendados
form
syrup
Quality Level
optical activity
[α]20/D -16.4 to -9.8 °, c = 2% (w/v) in water
concentration
≥60%
storage temp.
2-8°C
SMILES string
O[C@H]1COC(O)[C@@H]1O
InChI
1S/C4H8O4/c5-2-1-8-4(7)3(2)6/h2-7H,1H2/t2-,3+,4?/m0/s1
InChI key
FMAORJIQYMIRHF-URORKIPUSA-N
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Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
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Gertjan J M den Hartog et al.
Nutrition (Burbank, Los Angeles County, Calif.), 26(4), 449-458 (2009-07-28)
Hyperglycemia, oxidative stress, and the onset and progression of diabetic complications are strongly linked. Reduction of oxidative stress could be of utmost importance in the long-term treatment of diabetic patients. The chronic nature of the disease calls for a mode
Marc-Olivier Ebert et al.
Journal of the American Chemical Society, 130(45), 15105-15115 (2008-10-22)
TNA (alpha-( l)-threofuranosyl-(3'-2') nucleic acid) is a nucleic acid in which the ribofuranose building block of the natural nucleic acid RNA is replaced by the tetrofuranose alpha-( l)-threose. This shortens the repetitive unit of the backbone by one bond as
Laurence Burroughs et al.
Chemical communications (Cambridge, England), 46(26), 4776-4778 (2010-05-21)
Esters of proteinogenic amino acids efficiently catalyse the formation of erythrose and threose under aqueous conditions in the highest yields and enantioselectivities yet reported. Remarkably while esters of (L)-proline yield (L)-carbohydrates, esters of (L)-leucine and (L)-alanine generate (D)-carbohydrates, offering the
Mathias Ferencic et al.
Chemistry & biodiversity, 1(7), 939-979 (2006-12-29)
As part of a project that aims at screening TNA-related oligonucleotide systems in which threose backbone units may have some or all of their oxygen functions replaced by nitrogen, two TNA analogs containing (2'NH)- and (3'NH)-phosphoramidate groups, respectively, in place
Ying-Wei Yang et al.
Journal of molecular evolution, 65(3), 289-295 (2007-09-11)
Systematic investigation into the chemical etiology of ribose has led to the discovery of glycerol nucleic acid (GNA) and threose nucleic acid (TNA) as possible progenitor candidates of RNA in the origins of life. Coupled with their chemical simplicity, polymers
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