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Benzaldehyde, 2-hydroxy-, methylhydrazone, also known as salicylaldehyde methylhydrazone, is an organic compound with the chemical formula C9H12N2O. It is a derivative of benzaldehyde, where the aldehyde group is replaced by a hydrazone group, and a hydroxyl group is present at the 2-position on the benzene ring. Benzaldehyde, 2-hydroxy-, methylhydrazone is a colorless to pale yellow solid and is soluble in common organic solvents such as ethanol and acetone. It is synthesized by reacting salicylaldehyde with methylhydrazine, and it is used as an intermediate in the preparation of various pharmaceuticals and chemical compounds. Due to its reactivity and potential applications, salicylaldehyde methylhydrazone is an important compound in the field of organic chemistry.

4548-88-3

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4548-88-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4548-88-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,4 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4548-88:
(6*4)+(5*5)+(4*4)+(3*8)+(2*8)+(1*8)=113
113 % 10 = 3
So 4548-88-3 is a valid CAS Registry Number.

4548-88-3Downstream Products

4548-88-3Relevant academic research and scientific papers

Diazaborines oxidize slowly with H2O2 but rapidly with peroxynitrite in aqueous buffer

Domaille, Dylan W.,Golzwarden, Julian V. A.,Haggett, Jack G.,Han, Gun Su,Moser, Angela R.,Vyas, Shubham

supporting information, p. 995 - 999 (2022/02/16)

Reactive oxygen species (ROS) such as hydrogen peroxide (H2O2) and peroxynitrite (ONOO?) oxidize arylboronic acids to their corresponding phenols. When used in molecular imaging probes and in ROS-responsive molecules, however, simple arylboronic acids struggle to discriminate between H2O2 and ONOO? because of their fast rate of reaction with both ROS. Here, we show that diazaborines (DABs) react slowly with H2O2 but rapidly with peroxynitrite in an aqueous buffer. In addition to their slow reaction with H2O2, the immediate product of DAB oxidation with H2O2 and ONOO? can yield a kinetically trapped CN Z-isomer that slowly equilibrates with its E-isomer. Taken together, our work shows that diazaborines exhibit enhanced kinetic discrimination between H2O2 and ONOO? compared to arylboronic acids, opening up new opportunities for diazaborine-based tools in chemical biology.

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