Zolmitriptan impurity I is a pharmaceutical intermediate used as a reference standard for zolmitriptan impurity testing. It is a chemical compound related to the triptan class of drugs and is employed in quality control and research settings to ensure the purity of zolmitriptan active pharmaceutical ingredients.
콘텐츠 범위: 이 페이지의 정보는 화학물질 식별 및 산업 공급·연구개발·제조 맥락을 대상으로 합니다. 치료 효능 주장, 의료 조언 또는 의약품 사용 지침에 해당하지 않습니다.
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CAS 659738-69-9
2-methyl-1,4-diazepane
Pharmaceutical intermediate for rho kinase inhibitors
4,4'-BIPHENYLDICARBOXALDEHYDE
Pharmaceutical intermediate for organic synthesis
Diethylamine hydrochloride
pharmaceutical intermediate
2-Chloro-3-cyanopyridine
pharmaceutical intermediate
Zolmitriptan
active pharmaceutical ingredient
3-[2-(dimethylamino)ethyl]-5-[[(4S)-2-oxo-1,3-oxazolidin-4-yl]methyl]-1H-indole-2-carboxylic acid
PRLUPEADUDNTPI-NSHDSACASA-N
CN(C)CCC1=C(NC2=C1C=C(C=C2)C[C@H]3COC(=O)N3)C(=O)O