
CAS 1346600-85-8
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7 prodotti.
Zolpidem Related Compound A (N,N-Dimethyl-2-[7-methyl-2-p-tolylimidazo[1,2-a]pyridin-3-yl]acetamide)
CAS:Drugs with nitrogen hetero-atom(s) only, aromatic or modified aromatic, nesoiFormula:C19H21N3OColore e forma:Off-White PowderPeso molecolare:307.16846Zolpidem EP Impurity A (Zolpidem USP Related Compound A)
CAS:Formula:C19H21N3OColore e forma:White To Off-White SolidPeso molecolare:307.40N,N-Dimethyl-2-[7-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]acetamide
CAS:Prodotto controllatoFormula:C19H21N3OColore e forma:NeatPeso molecolare:307.395-Methyl Zolpidem
CAS:Prodotto controllato<p>Applications An impurity of Zolpidem (Z650000).<br></p>Formula:C19H21N3OColore e forma:NeatPeso molecolare:307.395-Methyl Zolpidem
CAS:<p>5-Methyl Zolpidem is a zolpidem tartrate that is used for the treatment of insomnia and as a sedative. It is an intermediate in the synthesis of zolpidem tartrate, which is synthesized from 5-methyl-1-(4-methoxybenzoyl)-1H-benzo[d]imidazole with potassium t-butoxide. The synthesis starts with the conversion of 5-methyl-1-(4-methoxybenzoyl)-1H-benzo[d]imidazole to 1-(4'-methylphenyl) benzene by reaction with methyl iodide followed by hydrolysis of the ester group to form 1-(4'-methylphenyl) benzene. The next step involves a nucleophilic substitution reaction using potassium t-butoxide to produce 1-(4'-methylphenyl) benzene t-butoxide, followed by reaction with methanol</p>Formula:C19H21N3OPurezza:Min. 95%Colore e forma:White/Off-White SolidPeso molecolare:307.39 g/molRef: ST-EA-CP-Z1001
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