Weight | 166.132 g/mol |
---|---|
Formula | C8H6O4 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
1,3-benzodioxole-4-carboxylic acid (5768-39-8)
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- Synthesis of (S)-(+)-2-tert-butyl-2-methyl-1,3-benzodioxole-4-carboxylic acid: A new type chiral derivation reagent for amines and alcohols (Tetrahedron Letters, 1989)
- (+)-Tert-butyl-1,3-benzodioxole-4-carboxylic acid: Fluorescent chiral carboxylic acid with a 1,3-benzodioxole skeleton (Tetrahedron-asymmetry, 1993)
- Simultaneous Analysis of Enantiomeric Amino Acids Based on Derivatization with (S)-(+)-2-t-Butyl-2-methyl-1,3-benzodioxole-4-carboxylic Acid and High-Performance Liquid Chromatography. (Analytical Sciences, 1996)
- Simple and highly sensitive high-performance liquid chromatographic method for separating enantiomeric diacylglycerols by direct derivatization with a fluorescent chiral agent, (S)-(+)-2-tert.-butyl-2-methyl-1,3-benzodioxole-4-carboxylic acid (Journal of Chromatography A, 1995)
- Highly sensitive high-performance liquid chromatographic method to discriminate enantiomeric monoacylglycerols based on fluorescent chiral derivatization with (S)-(+)-2-tert.-butyl-2-methyl-1,3-benzodioxole-4-carboxylic acid (Journal of Chromatography A, 1995)
- Determination of the absolute configuration of monosaccharides using (+) or () 2-tert-butyl-2-methyl-1,3-benzodioxole-4-carboxylic acid and high-resolution 1H-n.m.r. spectroscopy (Carbohydrate Research, 1991)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1OC2=CC=CC(=C2O1)C(=O)O
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InChIKeyDBUAYOWCIUQXQW-UHFFFAOYSA-N
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