| Weight | 185.02 g/mol |
|---|---|
| Formula | C7H5BrO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
3-Bromobenzaldehyde (3132-99-8)
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- PALLADIUM-CATALYZED SYNTHESIS OF 3-ALKYLPHTHALIDES VIA CARBONYLATIVE CYCLIZATION OF O-BROMOBENZALDEHYDE WITH 1,3-DICARBONYL COMPOUNDS (Synthetic Communications, 1997)
- PALLADIUM-CATALYZED SYNTHESIS OF 3-(ALKYLAMINO)ISOINDOLIN-1-ONES BY CARBONYLATIVE CYCLIZATION OF 2-BROMOBENZALDEHYDE WITH PRIMARY AMINES (Journal of Heterocyclic Chemistry, 1997)
- A facile synthesis of 3-alkoxy phthalides by the palladium catalyzed carbonylative cyclization of o-bromobenzaldehyde (Journal of Heterocyclic Chemistry, 1995)
- Facile Palladium-Catalyzed Synthesis of 3-oxo- 1,3-Dihydro-1-Isobenzofuranyl Alkanoates From 2-Bromobenzaldehyde and Carboxylic Acids (Synthetic Communications, 2000)
- Synthesis of 3phenoxy1,3dihydro1isobenzofuranones by palladiumcatalyzed carbonylative cyclization of 2bromobenzaldehyde with phenols (Journal of Heterocyclic Chemistry, 1999)
- PALLADIUM-CATALYZED SYNTHESIS OF 3-OXO-1,3-DIHYDRO-1-ISOBENZOFURANYL ALKANOATES FROM 2-BROMOBENZALDEHYDE AND SODIUM ALKANOATES (Journal of Heterocyclic Chemistry, 1999)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC(=CC(=C1)Br)C=O
-
InChIKeySUISZCALMBHJQX-UHFFFAOYSA-N
- Pubchem - 3-Bromobenzaldehyde
- Wikipedia - 3-formylbromobenzene
3-Bromobenzaldehyde is stable under normal temperature and pressure.
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(1074-24-4)
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3-Bromobenzaldehyde
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