| Weight | 185.02 g/mol |
|---|---|
| Formula | C7H5BrO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
2-Bromobenzaldehyde (6630-33-7)
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- Synthesis of substituted benzene derivatives by homo- and hetero-coupling of 2-bromobenzaldehyde and bromovinylaldehydes followed by McMurry coupling (Tetrahedron Letters, 2006)
- SYNTHESIS OF ISOINDOLINONES BY PALLADIUM-CATALYZED CARBONYLATIVE CYCLIZATION OF 2-BROMOBENZALDEHYDE WITH DIAMINES (Synthetic Communications, 1998)
- Palladium-catalyzed carbonylative cyclization of 2-bromobenzaldehyde with primary amines leading to isoindolin-1-ones (Tetrahedron Letters, 2009)
- PALLADIUM-CATALYZED SYNTHESIS OF 3-(ALKYLAMINO)ISOINDOLIN-1-ONES BY CARBONYLATIVE CYCLIZATION OF 2-BROMOBENZALDEHYDE WITH PRIMARY AMINES (Journal of Heterocyclic Chemistry, 1997)
- Configuration at the 2-position of oxazolidines derived from 1-ephedrine and p-bromobenzaldehyde: an X-ray structure redetermination (Journal of Organic Chemistry, 1983)
- Molecular orbital studies (hardness, chemical potential, electrophilicity, and first electron excitation), vibrational investigation and theoretical NBO analysis of 2-hydroxy-5-bromobenzaldehyde by density functional method (Journal of Molecular Structure, 2013)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C(=C1)C=O)Br
-
InChIKeyNDOPHXWIAZIXPR-UHFFFAOYSA-N
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