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Merck
CN

68854

Sigma-Aldrich

L-Arabino-1,4-lactone

≥95.0% (GC)

别名:

D-Arabinonic acid γ-lactone, L-Arabinono-1,4-lactone

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About This Item

经验公式(希尔记法):
C5H8O5
CAS号:
分子量:
148.11
Beilstein:
82060
MDL编号:
UNSPSC代码:
12352201
PubChem化学物质编号:
NACRES:
NA.25

质量水平

方案

≥95.0% (GC)

表单

powder

旋光性

[α]/D -72.0±8.0°, c = 1 in H2O

适用性

conforms to structure for Proton NMR spectrum

SMILES字符串

O=C1[C@H](O)[C@@H](O)[C@H](CO)O1

InChI

1S/C5H8O5/c6-1-2-3(7)4(8)5(9)10-2/h2-4,6-8H,1H2/t2-,3-,4+/m0/s1

InChI key

CUOKHACJLGPRHD-YVZJFKFKSA-N

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Medel Manuel L Zulueta et al.
Chemical communications (Cambridge, England), 49(32), 3275-3287 (2013-02-28)
Carbohydrates either conjugated or as free entities are major players in numerous biological processes. The desire to comprehend the nature of their functions and further develop therapeutic and diagnostic applications has fuelled the recent upsurge in the glycoscience field. Mainly
Ana S P Moreira et al.
Journal of mass spectrometry : JMS, 49(4), 280-290 (2014-04-11)
The oxidation of α-(1 → 5)-L-arabinotriose (Ara3), an oligosaccharide structurally related to side chains of coffee arabinogalactans, was studied in reaction with hydroxyl radicals generated under conditions of Fenton reaction (Fe(2+)/H2O2). The acidic and neutral oxidation products were separated by ligand exchange/size-exclusion
Dominik Mojzita et al.
FEBS letters, 584(16), 3540-3544 (2010-07-27)
L-Xylulose reductase is part of the eukaryotic pathway for l-arabinose catabolism. A previously identified L-xylulose reductase in Hypocrea jecorina turned out to be not the 'true' one since it was not upregulated during growth on L-arabinose and the deletion strain
Extraction of Hemicellulose from Loblolly Pine Woodchips and Subsequent Kraft Pulping.
Huang, F. and Ragauskas, A.
Industrial & Engineering Chemistry Research, 52, 1743-1749 (2013)
Robert M Archer et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(8), 2895-2902 (2013-01-15)
Practical syntheses of 2-keto-3-deoxy-D-xylonate (D-KDX) and 2-keto-3-deoxy-L-arabinonate (L-KDA) that rely on reaction of the anion of ethyl 2-[(tert-butyldimethylsilyl)oxy]-2-(dimethoxy phosphoryl) acetate with enantiopure glyceraldehyde acetonide, followed by global deprotection of the resultant O-silyl-enol esters, have been developed. This has enabled us

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