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Drug Intermediate
Drug Iintermediate
- [1]. Ma HC, et al. Homochiral Covalent Organic Framework for Catalytic Asymmetric Synthesis of a Drug Intermediate. J Am Chem Soc. 2020 Jul 22;142(29):12574-12578. [Content Brief]
- [2]. Ramachary D B, et al. Development of pharmaceutical drugs, drug intermediates and ingredients by using direct organo‐click reactions[J]. 2008.
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Drug Intermediate Related Products (4598)
Related Products (4598)
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N'-Hydroxy-3-methylbenzenecarboximidamide
0 ImagesCat. No.: HY-W144281CAS No.: 40067-82-1Synonyms: 3-MethylbenzamidoximeN'-Hydroxy-3-methylbenzenecarboximidamide is an intermediate useful for pharmaceutical synthesis. -
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Pitavastatin impurity 12
0 ImagesCat. No.: HY-21315CAS No.: 185105-98-0 -
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5,7-Dihydroxy-4-methylphthalide
0 Images5,7-Dihydroxy-4-methylphthalide is a key intermediate in the synthesis of Mycophenolic acid and a secondary metabolite of Aspergillus flavus. -
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1-tert-Butyl-3-ethoxybenzene
0 ImagesCat. No.: HY-75981CAS No.: 133073-81-11-tert-Butyl-3-ethoxybenzene is a drug intermediate for synthesis of various active compounds. -
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- Valproic acid impurity 1
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1-(2-Methoxyphenyl)piperazine hydrochloride
0 Images1-(2-Methoxyphenyl)piperazine hydrochloride is a key agent intermediate of antipsychotics with high affinity to the serotonin receptors and 5-HT, which can be used to synthesize the intestinal worm-repellent agents Piperazine phosphate (HY-B0912C) and Piperazine citrate (HY-17599), as well as Fluphenazine (HY-119980), dihydrochloride, Rifampicin (HY-B0272). -
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9-Propenyladenine
0 ImagesCat. No.: HY-100079CAS No.: 1446486-33-4Synonyms: Mutagenic impurity of tenofovir disoproxil9-Propenyladenine is a mutagenic impurity in tenofovir disoproxil fumarate. Tenofovir is an antiretroviral agent known as nucleotide analogue reverse transcriptase inhibitors, which block reverse transcriptase, a crucial virus enzyme in HIV-1 and HBV. -
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- 4-Biphenylmethanol
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D-Ribulose (1 M in water)
0 ImagesD-Ribulose (1 M in water) is a pentose sugar, a key intermediate in the Calvin cycle, and a substrate for pentose isomerase and ribulokinase. D-Ribulose (1 M in water) can be enzymatically converted to D-arabinose by pentose isomerase; it undergoes a two-step oxidation by cells of Acetobacter suboxydans. D-Ribulose (1 M in water) can be used in metabolism-related research. -
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- Ticagrelor impurity 27
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- 4-Methyl-3-hydroxyanthranilic acid
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FPPS ligand 3
0 ImagesCat. No.: HY-W100829CAS No.: 51527-19-6FPPS ligand 3 (compound 2) is a farnesyl pyrophosphate synthase (FPPS) ligand. FPPS ligand 3 binds to the hydrophobic base region of the FPPS pocket. FPPS ligand 3 can be used to design and synthesize FPPS inhibitors. -
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Nicotinoyl azide
0 ImagesNicotinoyl azide is capable of forming high energy intermediates known to form C-8 adducts with adenosine and guanosine. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. -
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Rotigotine impurity 2
0 ImagesCat. No.: HY-Z0731CAS No.: 32920-08-4 -
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Vonoprazan impurity 46
0 ImagesCat. No.: HY-Z3136CAS No.: 2169267-53-0 -
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Rosuvastatin impurity 47
0 ImagesCat. No.: HY-134526CAS No.: 355806-00-7Rosuvastatin impurity 47 is an impurity of Rosuvastatin. -
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- 2-Oxoarginine
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- Indobufen impurity 2
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UMP-morpholidate
0 ImagesUMP-morpholidate is an intermediate of pharmaceutical synthesis by coupling. -
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6-(2-Hydroxyethoxy)-1-hexanol
0 ImagesCat. No.: HY-22245CAS No.: 23684-16-46-(2-Hydroxyethoxy)-1-hexanol is a drug intermediate for synthesis of various active compounds. -
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