Weight | 201.019 g/mol |
---|---|
Formula | C7H5BrO2 |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
3-BROMOBENZOIC ACID (585-76-2)
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- Biochemically generated chiral intermediates for organic synthesis: The absolute stereochemistry of 4-bromo-cis-2,3-dihydroxycyclohexa-4,6-diene-1-carboxylic acid formed from 4-bromobenzoic acid by a mutant of pseudomonas putida. (Tetrahedron Letters, 1987)
- Hydrogen Bromide-Acetic Acid Demethylation of 2,3-Dimethoxy-6-bromobenzoic Acid. An Example of Concomitant Bromine Migration1,2 (Journal of Organic Chemistry, 1960)
- Facile synthesis of isoindoline-1,3-diones by palladium-catalyzed carbonylative cyclization of o -bromobenzoic acid and primary amines (Frontiers of Chemical Engineering in China, 2013)
- Crystal structure of 2-amino-3-bromobenzoic acid, C7H6BrNO2, at 173 K (Zeitschrift Fur Kristallographie-new Crystal Structures, 2010)
- Rearrangement of Bromine Atom in the Demethylation of Bromomethoxybenzoic Acid. III.: 2-Bromoveratric Acid and 3-Methoxy-6-bromobenzoic Acid@@@2-Bromoveratric Acid3-Methoxy-6-bromobenzoic Acid (Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan, 1956)
- Process for preparing 3,5-dihydroxy 4-bromobenzoic acid (1996)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC(=C1)Br)C(=O)O
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InChIKeyVOIZNVUXCQLQHS-UHFFFAOYSA-N
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