
CAS 1346600-85-8
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7 produits concernés.
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, nesoiFormule :C19H21N3OCouleur et forme :Off-White PowderMasse moléculaire :307.16846Zolpidem EP Impurity A (Zolpidem USP Related Compound A)
CAS :Formule :C19H21N3OCouleur et forme :White To Off-White SolidMasse moléculaire :307.40N,N-Dimethyl-2-[7-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]acetamide
CAS :Produit contrôléFormule :C19H21N3OCouleur et forme :NeatMasse moléculaire :307.395-Methyl Zolpidem
CAS :Produit contrôlé<p>Applications An impurity of Zolpidem (Z650000).<br></p>Formule :C19H21N3OCouleur et forme :NeatMasse moléculaire :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>Formule :C19H21N3ODegré de pureté :Min. 95%Couleur et forme :White/Off-White SolidMasse moléculaire :307.39 g/mol







