Date published: 2026-4-30

1-800-457-3801

SCBT Portrait Logo
Seach Input

2-Bromo-3-hydroxybenzaldehyde (CAS 196081-71-7)

0.0(0)
Write a reviewAsk a question

CAS Number:
196081-71-7
Molecular Weight:
201.02
Molecular Formula:
C7H5BrO2
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

2-Bromo-3-hydroxybenzaldehyde is soluble in water and ethanol. This compound has found application in scientific research, notably in synthesizing novel compounds, probing biochemical pathways, and investigating chemical reactivity. As a reagent, it facilitates the synthesis of diverse compounds, including 2-bromo-3-hydroxybenzoic acid and 3-bromo-2-hydroxybenzoic acid. Additionally, it has been instrumental in studying biochemical pathways and exploring the reactivity of aldehydes with nucleophiles.


2-Bromo-3-hydroxybenzaldehyde (CAS 196081-71-7) References

  1. New chiral benzothiazine ligand and its use in the synthesis of a chiral receptor.  |  Harmata, M., et al. 2006. J Org Chem. 71: 3650-2. PMID: 16626160
  2. Enantioselective Synthesis of Both Epimers at C-21 in the Proposed Structure of Cytotoxic Macrolide Callyspongiolide.  |  Ghosh, AK. and Kassekert, LA. 2016. Org Lett. 18: 3274-7. PMID: 27331421
  3. Enantioselective total synthesis and structural assignment of callyspongiolide.  |  Ghosh, AK., et al. 2016. Org Biomol Chem. 14: 11357-11370. PMID: 27762414
  4. Enantioselective Synthesis of the Unsaturated Fragment of Callyspongiolide.  |  Matoušová, E., et al. 2016. Org Lett. 18: 5656-5659. PMID: 27783529
  5. Exploration of Biaryl Carboxylic Acids as Proton Shuttles for the Selective Functionalization of Indole C-H Bonds.  |  Pi, JJ., et al. 2018. J Org Chem. 83: 5791-5800. PMID: 29664291
  6. Structure Guided Design, Synthesis, and Biological Evaluation of Novel Benzosuberene Analogues as Inhibitors of Tubulin Polymerization.  |  Niu, H., et al. 2019. J Med Chem. 62: 5594-5615. PMID: 31059248
  7. Silver-Mediated Synthesis of Substituted Benzofuran- and Indole-Pyrroles via Sequential Reaction of ortho-Alkynylaromatics with Methylene Isocyanides.  |  Liu, JQ., et al. 2019. J Org Chem. 84: 8998-9006. PMID: 31117557
  8. Synthetic Studies toward Bazzanin K: Regioselective and Chemoselective Three-Component Suzuki Coupling.  |  Ju, X., et al. 2019. J Org Chem. 84: 12246-12252. PMID: 31448911
  9. Synthesis of the Tetracyclic Framework of Polycyclic Spiro Lignan Natural Products.  |  Ali, G. and Cuny, GD. 2020. ACS Omega. 5: 9007-9012. PMID: 32337465
  10. Synthesis and Structure-Activity Relationships of Aristoyagonine Derivatives as Brd4 Bromodomain Inhibitors with X-ray Co-Crystal Research.  |  Yoo, M., et al. 2021. Molecules. 26: PMID: 33802888
  11. Expanding Benzoxazole-Based Inosine 5'-Monophosphate Dehydrogenase (IMPDH) Inhibitor Structure-Activity As Potential Antituberculosis Agents.  |  Chacko, S., et al. 2021. J Med Chem. 64: 18233-18234. PMID: 34855408
  12. Alkyne Insertion Enabled Vinyl to Acyl 1,5-Palladium Migration: Rapid Access to Substituted 5-Membered-Dihydrobenzofurans and Indolines.  |  Ding, M., et al. 2023. Angew Chem Int Ed Engl. 62: e202300703. PMID: 36808789

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Bromo-3-hydroxybenzaldehyde, 1 g

sc-265449
1 g
$101.00

2-Bromo-3-hydroxybenzaldehyde, 5 g

sc-265449A
5 g
$392.00