CAS 618-49-5
:3-Hydroxybenzamide
Description:
3-Hydroxybenzamide, also known as meta-hydroxybenzamide, is an organic compound characterized by the presence of a hydroxyl group (-OH) and an amide functional group (-C(=O)NH2) attached to a benzene ring. Its molecular structure features a benzene ring with the hydroxyl group positioned at the meta position relative to the amide group. This compound is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to its ability to form hydrogen bonds. 3-Hydroxybenzamide exhibits various chemical properties, including the potential to participate in hydrogen bonding and act as a weak acid due to the hydroxyl group. It is often used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals and agrochemicals. Additionally, its derivatives can exhibit biological activity, making it of interest in medicinal chemistry. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.
Formula:C7H7NO2
InChI:InChI=1/C7H7NO2/c8-7(10)5-2-1-3-6(9)4-5/h1-4,9H,(H2,8,10)
InChI key:InChIKey=NGMMGKYJUWYIIG-UHFFFAOYSA-N
SMILES:C(N)(=O)C1=CC(O)=CC=C1
Synonyms:- 3-Hydroxy-Benzoic Acid,Amide
- 3-Hydroxy-benzamide
- 3-Hydroxybenzenecarboxamide
- 3-Hydroxyphenylformamide
- Benzamide, 3-Hydroxy-
- Benzamide, m-hydroxy-
- NSC 379289
- Sr 4267
- m-Hydroxybenzamide
- 3-Hydroxybenzamide
- 1-phenyl-5-(4-phenylphenyl)-3-pyrazolecarboxylic acid methyl ester
- See more synonyms
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Found 5 products.
3-Hydroxybenzamide
CAS:Formula:C7H7NO2Purity:>98.0%(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:137.143-Hydroxybenzamide
CAS:<p>3-Hydroxybenzamide is a potent inhibitor of the enzyme synthetase and has been shown to inhibit the synthesis of adenosine diphosphate (ADP) ribose. It has been shown to have potent inhibitory activity against the enzyme in both solid and liquid phases. 3-Hydroxybenzamide binds to the carbonyl group of ADP ribose, which prevents it from binding to ATP. This inhibition of the synthesis of nucleotides limits cell proliferation by preventing DNA replication and protein synthesis. 3-Hydroxybenzamide has also been shown to inhibit the growth of mouse leukemia cells in vitro, as well as inhibiting l1210 murine leukemia cells grown in vivo. The mechanism for this inhibition is not yet known, but may be due to its ability to bind with hydrogen bonds or intramolecular hydrogen bonds. 3-Hydroxybenzamide also has a skeleton that can be synthesized asymmetrically by using a chiral</p>Formula:C7H7NO2Purity:Min. 95%Color and Shape:PowderMolecular weight:137.14 g/mol
