Date published: 2025-12-19

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10-Chloro-9-anthraldehyde (CAS 10527-16-9)

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CAS Number:
10527-16-9
Purity:
≥95%
Molecular Weight:
240.68
Molecular Formula:
C15H9ClO
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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10-Chloro-9-anthraldehyde, also known as 10-Cl-9-Ald, is an artificial compound classified as an aldehyde. It appears as a colorless, crystalline solid, weighing 240.68 g/mol. This compound, with its versatile properties, serves as a valuable reagent in the realm of organic synthesis. Its potential applications extend to multiple fields, including medicine, materials science, and biochemistry. In materials science, 10-Chloro-9-anthraldehyde finds utility in synthesizing polymers and other materials. Similarly, in the field of biochemistry, it contributes to the synthesis of enzymes and other biomolecules. Although the precise mechanism of action for 10-Chloro-9-anthraldehyde remains unclear, it is known to engage in reactions with diverse compounds, resulting in the creation of novel compounds that can be employed across various applications.


10-Chloro-9-anthraldehyde (CAS 10527-16-9) References

  1. Antimalarial amino alcohols II: anthraceneaminoethanols and anthraceneaminopropanols (1- and 9-substituted).  |  Traxler, JT., et al. 1975. J Pharm Sci. 64: 1943-9. PMID: 1107515
  2. Innovative sol-gel coatings for solid-phase microextraction. Development of fibers for the determination of polycyclic aromatic hydrocarbons at trace level in water.  |  Bianchi, F., et al. 2008. J Chromatogr A. 1196-1197: 15-22. PMID: 18258246
  3. Design and synthesis of novel photoinduced electron transfer-based hybridization probes.  |  Yokoyama, C., et al. 2017. Bioorg Med Chem. 25: 3574-3582. PMID: 28522268
  4. Amphiphilic lysine conjugated to tobramycin synergizes legacy antibiotics against wild-type and multidrug-resistant Pseudomonas aeruginosa.  |  Lyu, Y., et al. 2017. Biopolymers.. PMID: 29205266
  5. A hypoxia-activated antibacterial prodrug.  |  Yeoh, YQ., et al. 2020. Bioorg Med Chem Lett. 30: 127140. PMID: 32247730
  6. Antimalarial activities of some 3,5-diamino-as-triazine derivatives.  |  Rees, RW., et al. 1972. J Med Chem. 15: 859-61. PMID: 5044307
  7. Synthesis of halogenated anthraldehydes and their conversion to antimalarial amino alcohols.  |  Traxler, JT., et al. 1972. J Med Chem. 15: 861-3. PMID: 5044308
  8. 3-Chromanamine hydrochlorides with central stimulant activity.  |  Lockhart, IM. and Foard, SA. 1972. J Med Chem. 15: 863-5. PMID: 5044309
  9. Steric effects on aldehyde group relaxation in some aromatic aldehydes  |  Lakshmi, A., Walker, S., Weir, N. A., & Calderwood, J. H. 1978. The Journal of Physical Chemistry. 82(9): 1091-1095.
  10. Intramolecular Diels-Alder additions. 1. Additions to anthracene and acridine  |  Ciganek, E. 1980. The Journal of Organic Chemistry. 45(8): 1497-1505.
  11. Role of ion pairs in the photochemistry of electron donor-acceptor complexes. Picosecond spectroscopic studies of arene-tetracyanoethylene systems  |  Hilinski, E. F., Masnovi, J. M., Kochi, J. K., & Rentzepis, P. M. 1984. Journal of the American Chemical Society. 106(26): 8071-8077.
  12. Utilization of flow chemistry in catalysis: New avenues for the selective synthesis of Bis (indolyl) methanes  |  Mohapatra, S. S., Wilson, Z. E., Roy, S., & Ley, S. V. 2017. Tetrahedron. 73(14): 1812-1819.
  13. DNA and BSA interaction studies and antileukemic evaluation of polyaromatic thiosemicarbazones and their copper complexes  |  Pelosi, G., Pinelli, S., & Bisceglie, F. 2022. Compounds. 2(2): 144-162.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

10-Chloro-9-anthraldehyde, 1 g

sc-223140
1 g
$117.00