assay
98%
mp
73-75 °C (lit.)
SMILES string
CCC(C)(O)C(O)=O
InChI
1S/C5H10O3/c1-3-5(2,8)4(6)7/h8H,3H2,1-2H3,(H,6,7)
InChI key
MBIQENSCDNJOIY-UHFFFAOYSA-N
Application
2-Hydroxy-2-methylbutyric acid can be used as:
- A complexing agent in a new electrolytic system, applicable in the isotachophoretic lanthanide separation.
- An aldehyde surrogate to prepare pyrrolo[1,2-a]quinoxaline derivatives by reacting with 2-(1H-pyrrol-1-yl)aniline.
- A starting material to synthesize Cr(V) reagent named sodium bis(2-hydroxy-2-methylbutyrato)oxochromate(V) (Aldrich cat. no. ALD00006) applicable in the total synthesis of (−)-taxuyunnanine D.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
α-Hydroxy acid as an aldehyde surrogate: metal-free synthesis of pyrrolo [1, 2-a] quinoxalines, quinazolinones, and other N-heterocycles via decarboxylative oxidative annulation reaction
Viji M, et al.
Royal Society of Chemistry Advances, 10(61), 37202-37208 (2020)
W Dekant et al.
Research report (Health Effects Institute), (102)(102), 29-71 (2001-08-16)
The biotransformation of methyl tert-butyl ether (MTBE), ethyl tert-butyl ether (ETBE), and tert-amyl methyl ether (TAME) was studied in humans and in rats after inhalation of 4 and 40 ppm of MTBE, ETBE, and TAME, respectively, for 4 hours, and
Two-phase synthesis of (−)-taxuyunnanine D
Wilde NC, et al.
Journal of the American Chemical Society, 136(13), 4909-4912 (2014)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| H40009-5G | 04061831826999 |
