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About This Item
Empirical Formula (Hill Notation):
C6H10O3
CAS Number:
Molecular Weight:
130.14
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4659425
Assay:
97%
Form:
crystals
Quality Level
assay
97%
form
crystals
optical activity
[α]22/D +50.0°, c = 0.5 in H2O
bp
120-122 °C/15 mmHg (lit.)
mp
89-93 °C
functional group
ester, hydroxyl
storage temp.
2-8°C
SMILES string
CC1(C)COC(=O)[C@H]1O
InChI
1S/C6H10O3/c1-6(2)3-9-5(8)4(6)7/h4,7H,3H2,1-2H3/t4-/m1/s1
InChI key
SERHXTVXHNVDKA-SCSAIBSYSA-N
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Zhiqiang Liu et al.
Journal of agricultural and food chemistry, 54(16), 5823-5830 (2006-08-03)
D-Pantonohydrolase has attracted increasing attention as a biocatalyst for stereospecific production of D-pantoic acid. The Fusarium moniliforme D-pantonohydrolase was selected for directed evolution through error-prone Polymerase Chain Reaction (PCR) combined with DNA shuffling for improved activity and pH stability using
Total synthesis and antitumor activity of ZK-EPO: the first fully synthetic epothilone in clinical development.
Ulrich Klar et al.
Angewandte Chemie (International ed. in English), 45(47), 7942-7948 (2006-09-29)
A D Keefe et al.
Nature, 373(6516), 683-685 (1995-02-23)
The involvement of coenzyme A in many enzyme reactions suggests that it acted in this capacity very early in the development of life on Earth. Particularly relevant in this regard is its role in the activation of amino acids and
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 729698-1G | 04061826653289 |
