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  • CAS 1260251-26-0 | BIRI-010 : Birinapant
    (World's Largest Pharmaceutical Supplier)

    CAS Number: 1260251-26-0
    Stock: 999g
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CAS Number:1260251-26-0
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SMILES:IntroductionProperties of CAS 1260251-26-0Synthesis of CAS 1260251-26-0Uses of CAS 1260251-26-0ConclusionIntroductionCAS 1260251-26-0, also known as (2S,3S)-3-(2,6-dimethylphenyl)-2-hydroxy-2-methoxypropanoic acid, is a chemical compound that belongs to the class of organic compounds known as phenylpropanoic acids. It is a white to off-white powder with a molecular formula of C12H16O4 and a molecular weight of 224.26 g/mol.Properties of CAS 1260251-26-0CAS 1260251-26-0 has a melting point of 122-124??C and a boiling point of 389.2??C at 760 mmHg. It is soluble in water and ethanol but insoluble in ether and chloroform. Its density is 1.22 g/cm3, and it has a refractive index of 1.537.Synthesis of CAS 1260251-26-0CAS 1260251-26-0 can be synthesized through a multi-step process starting with 2,6-dimethylphenol, which is converted into its corresponding methyl ether. The methyl ether is then subjected to a Friedel-Crafts acylation reaction with ethyl chloroformate in the presence of aluminum chloride, resulting in the formation of ethyl 2,6-dimethylphenylglyoxylate. This compound is then reduced with sodium borohydride to yield ethyl (2,6-dimethylphenyl) hydroxyacetate. Finally, this compound is hydrolyzed with sodium hydroxide to give CAS 1260251-26-0.Uses of CAS 1260251-26-0CAS 1260251-26-0 has been found to have potential therapeutic applications. It has been shown to exhibit anti-inflammatory and analgesic effects in animal models, making it a potential candidate for the treatment of pain and inflammation. Additionally, it has been reported to have antioxidant properties, which could make it a useful ingredient in cosmetic and skincare products.ConclusionIn conclusion, CAS 1260251-26-0 is a chemical compound with potential therapeutic applications due to its anti-inflammatory, analgesic, and antioxidant properties. Its synthesis involves a multi-step process starting with 2,6-dimethylphenol. Further research is needed to fully understand the potential applications of this compound.

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