Weight | 160.169 g/mol |
---|---|
Formula | C7H12O4 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 4 |
2,2-DIMETHYLGLUTARIC ACID (681-57-2)
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- Bifunctional chiral synthons via microbiological methods. 1. Optically active 2,4-dimethylglutaric acid monomethyl esters (Journal of the American Chemical Society, 1981)
- New nonenzymic chiral induction. A highly regioselective differentiation between two identical groups in meso-2,4-dimethylglutaric acid (Journal of Organic Chemistry, 1983)
- Synthesis of 2,4-dimethylglutaric acid monoesters via enzyme-catalyzed asymmetric alcoholysis of meso-2,4-dimethylglutaric anhydride (Tetrahedron-asymmetry, 1993)
- Radiolysis of the poly(acrylic acid) model 2,4-dimethylglutaric acid: a pulse radiolysis and product study (Journal of The Chemical Society-perkin Transactions 1, 1996)
- Enzymes in organic synthesis, 19. The enzyme-catalyzed sequential esterification of ()-anti-2,4-dimethylglutaric anhydride. An efficient route to enantiomerically enriched mono- and diesters of anti-2,4-dimethylglutaric acid (European Journal of Organic Chemistry, 1994)
- Model compounds of poly(methyl methacrylate). Conformational structure of the dimethyl esters of 2,2,4-trimethyl- and of 2-methoxymethyl-2,4-dimethylglutaric acid. 13C NMR, 1H NMR and vibrational spectroscopic study (Macromolecular Chemistry and Physics, 1985)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)(CCC(=O)O)C(=O)O
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InChIKeyBTUDGPVTCYNYLK-UHFFFAOYSA-N
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