CAS 6635-24-1
:3,4,5-tris(acetyloxy)benzoic acid
Description:
3,4,5-Tris(acetyloxy)benzoic acid, with the CAS number 6635-24-1, is an organic compound characterized by the presence of three acetyloxy groups attached to a benzoic acid structure. This compound features a benzene ring substituted at the 3, 4, and 5 positions with acetyl ester functional groups, which significantly influence its chemical properties. The presence of these acetyloxy groups enhances the compound's solubility in organic solvents and may affect its reactivity, particularly in esterification and hydrolysis reactions. As a benzoic acid derivative, it retains the acidic properties typical of carboxylic acids, allowing it to participate in acid-base reactions. Additionally, the acetyloxy groups can provide sites for further chemical modifications, making it a versatile intermediate in organic synthesis. The compound may also exhibit biological activity, although specific applications or effects would depend on further research. Overall, 3,4,5-tris(acetyloxy)benzoic acid is a notable compound in the realm of organic chemistry, particularly in the synthesis of more complex molecules.
Formula:C13H12O8
InChI:InChI=1/C13H12O8/c1-6(14)19-10-4-9(13(17)18)5-11(20-7(2)15)12(10)21-8(3)16/h4-5H,1-3H3,(H,17,18)
SMILES:CC(=O)Oc1cc(cc(c1OC(=O)C)OC(=O)C)C(=O)O
Synonyms:- 3,4,5-Triacetoxy-benzoic acid
- 3,4,5-Triacetoxybenzoic Acid
- Benzoic acid, 3,4,5-tris(acetyloxy)-
- 3,4,5-Tris(acetyloxy)benzoic acid
- GALLIC ACID TRIACETATE
- 3,4,5-TRIACETOXYBENZOIC ACID 97%
- RARECHEM AL BE 0488
- See more synonyms
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Found 4 products.
3,4,5-Tris(acetyloxy)benzoic acid
CAS:3,4,5-Tris(acetyloxy)benzoic acidPurity:95%Molecular weight:296.23g/mol3,4,5-tris(Acetyloxy)benzoic Acid
CAS:Controlled ProductFormula:C13H12O8Color and Shape:NeatMolecular weight:296.223,4,5-Triacetoxybenzoic acid
CAS:<p>Trifluoroacetic acid is an organic acid that is used in the synthesis of esters, ethers, and amides. It can be used to produce 3,4,5-triacetoxybenzoic acid (TABA), which inhibits the proliferation of leukemia cells. TABA binds to the active site of the protein runx2, which is involved in development and differentiation. It also inhibits vibrational spectra and chemical profiles that are related to cancer cell growth. TABA has been shown to induce autophagy through activation of AMPK signaling pathways in leukemia cells. TABA also inhibits lipid accumulation by inhibiting the expression of genes such as SREBP1c and ACC2.</p>Formula:C13H12O8Purity:Min. 97 Area-%Color and Shape:PowderMolecular weight:296.23 g/mol



