220477
D-(−)-Lyxose
99%
Sinônimo(s):
D-Lyxopyranose
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5 G
R$ 538,00
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5 G
R$ 538,00
About This Item
Fórmula empírica (Notação de Hill):
C5H10O5
Número CAS:
Peso molecular:
150.13
Beilstein:
1723083
Número CE:
Número MDL:
Código UNSPSC:
12352201
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Nível de qualidade
Ensaio
99%
atividade óptica
[α]25/D -15.8°, c = 4 in H2O
pf
108-112 °C (lit.)
cadeia de caracteres SMILES
O[C@@H]1COC(O)[C@@H](O)[C@H]1O
InChI
1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2/t2-,3+,4+,5?/m1/s1
chave InChI
SRBFZHDQGSBBOR-AGQMPKSLSA-N
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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M Jørgensen et al.
The Journal of organic chemistry, 66(13), 4625-4629 (2001-06-26)
The combination of a Wittig olefination and a dihydroxylation reaction constitutes a facile synthetic protocol for the transformation of unprotected carbohydrates into higher sugars. The Wittig reaction is carried out with tert-butyl or diphenylmethyl ester stabilized phosphoranes to give (E)-configured
Michal Letek et al.
PLoS genetics, 6(9), e1001145-e1001145 (2010-10-14)
We report the genome of the facultative intracellular parasite Rhodococcus equi, the only animal pathogen within the biotechnologically important actinobacterial genus Rhodococcus. The 5.0-Mb R. equi 103S genome is significantly smaller than those of environmental rhodococci. This is due to
H Wippo et al.
Bioorganic & medicinal chemistry, 9(9), 2411-2428 (2001-09-13)
The (L)-alpha-lyxopyranosyl-(4'-->3')-oligonucleotide system-a member of a pentopyranosyl oligonucleotide family containing a shortened backbone-is capable of cooperative base-pairing and of cross-pairing with DNA and RNA. In contrast, corresponding (D)-beta-ribopyransoyl-(4'-->3')-oligonucleotides do not show base-pairing under similar conditions. We conclude that oligonucleotide systems
M T Migawa et al.
Journal of medicinal chemistry, 41(8), 1242-1251 (1998-05-09)
Several 2-substituted alpha-D- and alpha-L-lyxofuranosyl and 5-deoxylyxofuranosyl derivatives of 5,6-dicholro-2-(isopropylamino)-1-(beta-L-ribofuranosyl) benzimidazole (1263W94) and 2,5,6-trichloro-1(beta-D-ribofuranosyl)benzimidazole (TCRB) were synthesized and evaluated for activity against two herpesviruses (HSV-1 and HCMV) and for their cytotoxicity against HFF and KB cells. Condensation of 1,2,3,5-tetra-O-acetyl-L-lyxofuranose (2a)
M Kern et al.
FEMS microbiology letters, 149(1), 31-37 (1997-04-01)
In this study the ability of various sugars and sugar alcohols to induce aldose reductase (xylose reductase) and xylitol dehydrogenase (xylulose reductase) activities in the yeast Candida tenuis was investigated. Both enzyme activities were induced when the organism was grown
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