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2,3-Pyrrolidinedione, 1-[(4-methoxyphenyl)methyl]-, commonly known as Mephenoxalone, is a chemical compound with the molecular formula C13H15NO3. It belongs to the class of organic compounds known as phenol ethers. Mephenoxalone is characterized by its muscle relaxant properties, which are utilized in the treatment of muscle pain and discomfort.

877776-88-0

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877776-88-0 Usage

Uses

Used in Pharmaceutical Industry:
Mephenoxalone is used as a muscle relaxant for the treatment of muscle pain or discomfort. It acts on the central nervous system to produce its relaxing effects, making it a valuable medication in the management of muscle-related conditions.
As a muscle relaxant, Mephenoxalone is available in various formulations such as tablets or capsules, allowing for convenient oral administration. It is important for patients to follow the prescribed dosage and adhere to any warnings or precautions provided by healthcare professionals to ensure safe and effective use.

Check Digit Verification of cas no

The CAS Registry Mumber 877776-88-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,7,7,7 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 877776-88:
(8*8)+(7*7)+(6*7)+(5*7)+(4*7)+(3*6)+(2*8)+(1*8)=260
260 % 10 = 0
So 877776-88-0 is a valid CAS Registry Number.

877776-88-0Downstream Products

877776-88-0Relevant academic research and scientific papers

Synthesis and reactivity with β-lactamases of a monobactam bearing a retro-amide side chain

Adediran,Lohier,Cabaret,Wakselman,Pratt

, p. 869 - 871 (2007/10/03)

The monobactam sodium 3-benzylcarbamoyl-2-oxo-1-azetidinesulfonate, bearing a retro (vs classical β-lactam)-amide side chain, has been synthesized and the kinetics of its reaction with typical β-lactamases studied. The new compound is generally a poorer substrate than the analogous compound with a normal side chain but its formation of a transiently stable complex with a class C β-lactamase sustains the retro-amide side-chain concept.

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