89796-22-5

Basic information

• Product Name: 1-(2-BROMO-ETHYL)-PIPERIDINE HYDROBROMIDE
• Synonyms: 1-(2-BROMO-ETHYL)-PIPERIDINE HYDROBROMIDE;Piperidine, 1-(2-bromoethyl)-, hydrobromide
• CAS NO: 89796-22-5
• Molecular Formula: BrH*C₇H₁₄BrN
• Molecular Weight: 273.01
• Mol File: 89796-22-5.mol
• Article Data: 5

Chemical Properties

• Melting Point: 219-220 °C(Solv: ethanol (64-17-5))
• Boiling Point: 207°Cat760mmHg
• Flash Point: 79°C
• Appearance: /
• Density: 1.295g/cm³
• Vapor Pressure: 0.23mmHg at 25°C
• Refractive Index: 1.501
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 1-(2-BROMO-ETHYL)-PIPERIDINE HYDROBROMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-BROMO-ETHYL)-PIPERIDINE HYDROBROMIDE(89796-22-5)
• EPA Substance Registry System: 1-(2-BROMO-ETHYL)-PIPERIDINE HYDROBROMIDE(89796-22-5)

Safety Data

• Hazardous Substances Data: 89796-22-5(Hazardous Substances Data)

Usage

General Description

1-(2-Bromo-ethyl)-piperidine hydrobromide is a chemical compound with the molecular formula C8H18Br2N2. It is a derivative of piperidine, a heterocyclic amine, and contains a bromo-ethyl group. 1-(2-BROMO-ETHYL)-PIPERIDINE HYDROBROMIDE is commonly used in organic synthesis and pharmaceutical research as a building block for the production of various pharmaceuticals and other biologically active compounds. It is typically available as a white to off-white crystalline solid and is soluble in water and ethanol. The hydrobromide salt form of 1-(2-Bromo-ethyl)-piperidine is commonly used as it makes the compound more stable and easier to handle. This chemical is primarily used as an intermediate in the synthesis of various drugs and other organic compounds.

InChI:InChI=1/C7H14BrN/c8-4-7-9-5-2-1-3-6-9/h1-7H2

Upstream product

• 3040-44-6 1-piperidinoethanol 
• 110-89-4 piperidine 

Downstream Products

• 1101118-83-5 N'-((5-cyanopyrazolo[1,5-a]pyridin-3-yl)methylene)-2-methyl-5-nitro-N-(2-(piperidin-1-yl)ethyl)benzenesulfonohydrazide 

Relevant articles and documents

Self-assembly of pseudo-rotaxane and rotaxane complexes using an electrostatic slippage approach

The protonation of a cyclic tertiary amine, integrated into the structure of a dumbbell-shaped guest molecule, accelerates the sliding of the guest through the cavity of a crown ether macrocycle to yield a stable pseudo-rotaxane complex. The use of an amine with the appropriate ring size followed by a proton transfer reaction leads to the formation of an interlocked rotaxane species.

Studies on 4(3H)-quinazolinone derivatives as antimalarials

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3-Aminoindazole derivatives

A compound of the formula (I): STR1 wherein W1 is a hydrogen atom or a STR2 group wherein Y is a C1-6 alkylene group or a C1-6 alkylene group having a C1-6 alkyl group substituent; and R1 and R2 each independently is a hydrogen atom or a C1-6 alkyl group and R1 and R2 may form a C4-6 heterocyclic ring or a nitrogen-containing C4-6 heterocyclic ring together with the adjacent nitrogen atom and the C4-6 heterocyclic rings may have at least one C1-6 alkyl group, hydroxyl group or halogen atom; W2 is a hydrogen atom or a STR3 group wherein Z is a C1-6 alkylene group or a C1-6 alkylene group having a C1-6 alkyl group substituent; and R3 and R4 each independently is a hydrogen atom or a C1-6 alkyl group and R3 and R4 may form a C4-6 heterocyclic ring or a nitrogen-containing C4-6 heterocyclic ring together with the adjacent nitrogen atom and the C4-6 heterocyclic rings may have at least one C1-6 alkyl group, hydroxyl group or halogen atom; when W1 is a hydrogen atom, W2 is the STR4 group; and when W2 is a hydrogen atom, W1 is the STR5 group; and the pharmaceutically acceptable acid addition salt thereof having antiinflammatory, analgesic and digestive tract ulcer suppressing activity.