Weight | 126.064 g/mol |
---|---|
Formula | C2H6O6 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Oxalic acid dihydrate (144-62-7, 6153-56-6)
Score:
#1393 in Physics
,
#4071 in Chemistry
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- A refinement of the crystal structure analyses of oxalic acid dihydrate (Acta Crystallographica, 1953)
- Effect of oxalic acid dihydrate on optical and electrochemical properties of solgel derived amorphous electrochromic WO3 films (Electrochimica Acta, 2005)
- 13C chemical shielding in oxalic acid, oxalic acid dihydrate, and diammonium oxalate (Journal of Chemical Physics, 1975)
- Wavefunctions derived from experiment. II. A wavefunction for oxalic acid dihydrate (Acta Crystallographica Section A, 2001)
- A practical and efficient synthesis of bis(indolyl)methanes in water, and synthesis of di-, tri-, and tetra(bis-indolyl)methanes under thermal conditions catalyzed by oxalic acid dihydrate (Molecular Diversity, 2010)
- Neutron diffraction study of hydrogen bonding and thermal motion in deuterated and oxalic acid dihydrate (Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry, 1969)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(=O)(C(=O)O)O.O.O
-
InChIKeyGEVPUGOOGXGPIO-UHFFFAOYSA-N
- Pubchem - Oxalic acid dihydrate
- Wikipedia - oxalic acid dihydrate
Oxalic acid is an organic compound with the formula C2H2O4. It is a colorless crystalline solid that forms a colorless solution in water. Its condensed formula is HOOCCOOH, reflecting its classification as the simplest dicarboxylic acid.
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Similar Compounds
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(563-63-3)
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acetate
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(623-50-7)
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(6000-43-7)
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(3926-62-3)
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