CAS 3086-62-2
:3,4,5-Trimethoxybenzamide
Description:
3,4,5-Trimethoxybenzamide is an organic compound characterized by its aromatic structure, featuring a benzene ring substituted with three methoxy groups (-OCH3) at the 3, 4, and 5 positions, along with an amide functional group (-C(O)NH2) attached to the benzene. This compound is typically a white to off-white solid and is soluble in organic solvents due to its hydrophobic methoxy groups, while its amide functionality can engage in hydrogen bonding, enhancing its solubility in polar solvents to some extent. The presence of multiple methoxy groups can influence its chemical reactivity, stability, and potential biological activity, making it of interest in various fields, including medicinal chemistry. 3,4,5-Trimethoxybenzamide may exhibit properties such as anti-inflammatory or analgesic effects, although specific biological activities would require further investigation. Its CAS number, 3086-62-2, is a unique identifier that facilitates the tracking and study of this compound in scientific literature and databases.
Formula:C10H13NO4
InChI:InChI=1/C10H13NO4/c1-13-7-4-6(10(11)12)5-8(14-2)9(7)15-3/h4-5H,1-3H3,(H2,11,12)
InChI key:InChIKey=GGNMTJKRHHLJHH-UHFFFAOYSA-N
SMILES:O(C)C1=C(OC)C=C(C(N)=O)C=C1OC
Synonyms:- Ai3-23424
- Benzamide, 3,4,5-trimethoxy-
- Brn 2697325
- Nsc 16947
- 3,4,5-Trimethoxybenzamide
- 4-10-00-02020 (Beilstein Handbook Reference)
- 3,4,5-trimethoxy-benzamid
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Found 6 products.
3,4,5-Trimethoxybenzamide
CAS:Formula:C10H13NO4Purity:>98.0%(HPLC)(N)Color and Shape:White to Almost white powder to crystalMolecular weight:211.22Benzamide, 3,4,5-trimethoxy-
CAS:Formula:C10H13NO4Purity:98%Color and Shape:SolidMolecular weight:211.21453,4,5-Trimethoxybenzamide
CAS:<p>3,4,5-Trimethoxybenzamide is a benzofuran that has been shown to have anti-cancer properties. It has been shown to inhibit the production of chemokines and inhibit cancer cell proliferation. 3,4,5-Trimethoxybenzamide also binds to chloride ion channels on cancer cells and blocks the influx of chloride ions into the cells. This causes an increase in intracellular pH and inhibits the formation of ATP. 3,4,5-Trimethoxybenzamide also has antiarrhythmic properties and can be used for the treatment of hypertension. It is metabolized by hydrolysis in tissues or blood pressure through piperidine formation or hydrochloric acid.</p>Formula:C10H13NO4Purity:Min. 95%Color and Shape:PowderMolecular weight:211.21 g/mol3,4,5-Trimethoxybenzamide
CAS:Formula:C10H13NO4Purity:98%Color and Shape:SolidMolecular weight:211.217





