CAS 22513-32-2

Benzohydroxamicacidsodiumsalt

Description:

Benzohydroxamic acid sodium salt, with the CAS number 22513-32-2, is a chemical compound that serves as a hydroxamic acid derivative. It is characterized by the presence of a hydroxamic functional group (-C(=O)N(OH)R) attached to a benzene ring, which contributes to its reactivity and solubility properties. This compound typically appears as a white to off-white solid and is soluble in water due to the ionic nature of the sodium salt. Benzohydroxamic acid derivatives are known for their ability to chelate metal ions, making them useful in various applications, including as inhibitors in enzymatic reactions and in the treatment of certain diseases. The compound may exhibit biological activity, particularly in relation to its interaction with metalloproteins. As with many chemical substances, safety precautions should be observed when handling it, as it may pose health risks if ingested or inhaled. Proper storage conditions should be maintained to ensure stability and prevent degradation.

Formula: C₇H₆NNaO₂

InChI: InChI=1/C7H6NO2.Na/c9-7(8-10)6-4-2-1-3-5-6;/h1-5H,(H-,8,9,10);/q-1;+1

Synonyms:

• Benzohydroxamic acdi sodium salt

Sodium Benzohydroxamate

CAS: 22513-32-2

Formula: C₇H₆NNaO₂

Purity: >98.0%(T)(HPLC)

Color and Shape: White to Orange to Green powder to crystal

Molecular weight: 159.12

Ref: 3B-B0112

Benzohydroxamic acid sodium salt

CAS: 22513-32-2

Formula: C₇H₆NNaO₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 159.1178

Ref: IN-DA003O2A

Sodium Benzohydroxamate Hydrate

CAS: 22513-32-2

Sodium Benzohydroxamate Hydrate

Purity: 97%

Ref: 54-OR1015012

Sodium Benzohydroxamate

CAS: 22513-32-2

Sodium benzohydroxamate (SBH) is a synthetic reagent that is used in organic synthesis to form hydroxamic acids. Sodium benzohydroxamate can be used as a substitute for sodium carbonate, which is not available in some countries. The reaction time of SBH and cyanamide is much shorter than the reaction time of sodium carbonate and cyanamide. The yield of hydroxamic acid formed by SBH is lower than the yield of hydroxamic acid formed by sodium carbonate, due to its low efficiency. Sodium hydrogen reacts with the cyanide ion to form the corresponding hydroxamic acid and ammonium ion, which are separated from each other during the process. A postulated mechanism for this reaction includes an aldehyde dehydrogenase enzyme that oxidizes the aldehyde group on the reactant, thereby forming an alcohol group.

Formula: C₇H₆NNaO₂

Purity: Min. 95%

Molecular weight: 159.12 g/mol

Ref: 3D-XAA51332