1571926-59-4

Basic information

• Product Name: C₃₃H₃₉F₂N₅O₆
• Synonyms: C₃₃H₃₉F₂N₅O₆
• CAS NO: 1571926-59-4
• Molecular Weight: 639.699
• Mol File: 1571926-59-4.mol

Chemical Properties

• CAS DataBase Reference: C₃₃H₃₉F₂N₅O₆(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₃H₃₉F₂N₅O₆(1571926-59-4)
• EPA Substance Registry System: C₃₃H₃₉F₂N₅O₆(1571926-59-4)

Safety Data

• Hazardous Substances Data: 1571926-59-4(Hazardous Substances Data)

Upstream product

• 159503-90-9 C₁₀H₁₇NO₃ 
• 387827-24-9 tert-butyl 4-[3-(acetylamino)-phenyl]-1-piperidinecarboxylate 
• 387827-20-5 tert-butyl 4-[3-(acetylamino)-phenyl]-1,2,3,6-tetrahydro-1-pyridinecarboxylate 
• 387827-25-0 N-[3-(piperidin-4-yl)phenyl]-acetamide 
• 1571926-57-2 prop-2-en-1-yl 3-[(3-bromopropyl)carbamoyl]-4-(3,4-difluorophenyl)-6-(methoxymethyl)-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate 
• 136637-38-2 5-(2-methoxyacetyl)-2,2-dimethyl-1,3-dioxane-4,6-dione 
• 1571926-55-0 prop-2-en-1-yl 4-(3,4-difluorophenyl)-6-(methoxymethyl)-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate 
• 387827-18-1 tert-butyl 4-[3-(amino)phenyl]-1,2,3,6-tetrahydro-1-pyridinecarboxylate 
• 138647-49-1 4-Trifluoromethanesulfonyloxy-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester 
• 79099-07-3 N-tert-butyloxycarbonylpiperidin-4-one 
• 1571926-54-9 prop-2-en-1-yl 4-methoxy-3-oxobutanoate 

Relevant articles and documents

Syntheses of precursors and reference compounds of the melanin- concentrating hormone receptor 1 (MCHR1) Tracers [11C]SNAP-7941 and [18F]FE@SNAP for positron emission tomography

The MCH receptor has been revealed as a target of great interest in positron emission tomography imaging. The receptor's eponymous substrate melanin-concentrating hormone (MCH) is a cyclic peptide hormone, which is located predominantly in the hypothalamus with a major influence on energy and weight regulation as well as water balance and memory. Therefore, it is thought to play an important role in the pathophysiology of adiposity, which is nowadays a big issue worldwide. Based on the selective and high-affinity MCH receptor 1 antagonist SNAP-7941, a series of novel SNAP derivatives has been developed to provide different precursors and reference compounds for the radiosyntheses of the novel PET radiotracers [11C]SNAP-7941 and [18F] FE@SNAP. Positron emission tomography promotes a better understanding of physiologic parameters on a molecular level, thus giving a deeper insight into MCHR1 related processes as adiposity.