337520-16-8

Basic information

• Product Name: t-Butyl 4-(2-bromo-4-nitrophenoxy)piperidine-1-carboxylate
• Synonyms: t-Butyl 4-(2-bromo-4-nitrophenoxy)piperidine-1-carboxylate;tert-Butyl 4-(2-broMo-4-nitrophenoxy)piperidine-1-carboxylate
• CAS NO: 337520-16-8
• Molecular Formula: C₁₆H₂₁BrN₂O₅
• Molecular Weight: 401.27
• Mol File: 337520-16-8.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: t-Butyl 4-(2-bromo-4-nitrophenoxy)piperidine-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: t-Butyl 4-(2-bromo-4-nitrophenoxy)piperidine-1-carboxylate(337520-16-8)
• EPA Substance Registry System: t-Butyl 4-(2-bromo-4-nitrophenoxy)piperidine-1-carboxylate(337520-16-8)

Safety Data

• Hazardous Substances Data: 337520-16-8(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
t-Butyl 4-(2-bromo-4-nitrophenoxy)piperidine-1-carboxylate is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and functional groups enable the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, t-Butyl 4-(2-bromo-4-nitrophenoxy)piperidine-1-carboxylate serves as an essential building block for the creation of novel agrochemicals. Its incorporation into the molecular structure of these compounds can enhance their effectiveness in pest control and crop protection.
Used in Organic Synthesis:
t-Butyl 4-(2-bromo-4-nitrophenoxy)piperidine-1-carboxylate is utilized as a versatile intermediate in organic synthesis. Its reactivity and functional groups allow for the formation of a wide range of organic compounds, expanding the scope of chemical research and development.
Used in Research and Development:
t-Butyl 4-(2-bromo-4-nitrophenoxy)piperidine-1-carboxylate is also employed in research and development settings, where its unique properties and reactivity are explored for potential applications in various fields. Its use in the synthesis of new compounds and the study of their properties can contribute to advancements in chemistry and related disciplines.

Upstream product

• 109384-19-2 t-butyl 4-hydroxy piperidine-1-carboxylate 

Downstream Products

• 337520-17-9 3-bromo-4-(1-t-butoxycarbonylpiperidin-4-yloxy)aniline 
• 1299487-31-2 1-(3-bromo-4-(1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yloxy)phenyl)-3-(tetrahydro-2H-pyran-4-yl)urea 
• 1299487-32-3 4-(2-bromo-4-nitrophenoxy)piperidine 
• 1299487-33-4 2-(4-((4-(2-bromo-4-nitrophenoxy)piperidin-1-yl)methyl)phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol 
• 1299487-34-5 2-(4-((4-(4-amino-2-bromophenoxy)piperidin-1-yl)methyl)phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol 

Relevant articles and documents

BENZAMIDINE DERIVATIVES

Benzamidine derivatives of formula (I) or pharmaceutically acceptable salts thereof exhibit excellent inhibitory activity against factor Xa and are useful for treating or preventing blood coagulation disorders: wherein R 1represents a hydrogen atom, a halogen atom, an alkyl group or a hydroxyl group; R 2represents a hydrogen atom, a halogen atom or an alkyl group, R 3represents a hydrogen atom, an optionally substituted alkyl group, an aralkyl group, an optionally substituted alkanoyl group or an optionally substituted alkylsulfonyl group, R 4and R 5 are the same as or different from each other and each represent a hydrogen atom, a halogen atom, an optionally substituted alkyl group, an alkoxy group, a carboxyl group, an alkoxycarbonyl group or an optionally substituted carbamoyl group, and R 6represents a substituted pyrrolidine group or substituted piperidine group.