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Merck
CN

T7642

L-(+)-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
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352201
EC Number:
202-419-6
MDL number:
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form

syrup

optical activity

[α]20/D 11.0 to 17.0, 48 hr, 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?/m1/s1

InChI key

FMAORJIQYMIRHF-BCDHYOAOSA-N

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.


存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

法规信息

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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
Alda Lisa Concia et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(15), 3808-3816 (2009-02-18)
Novel aldol addition reactions of dihydroxyacetone (DHA) and hydroxyacetone (HA) to a variety of aldehydes catalyzed by D-fructose-6-phosphate aldolase (FSA) are presented. In a chemical-enzymatic cascade reaction approach, 1-deoxynojirimycin and 1-deoxymannojirimycin were synthesized starting from (R)- and (S)-3-(N-Cbz-amino)-2-hydroxypropanal, respectively. Furthermore
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