1099597-60-0

Basic information

• Product Name: 1-Bromo-3-(3,3,3-trifluoropropyl)benzene
• Synonyms: 1-Bromo-3-(3,3,3-trifluoropropyl)benzene
• CAS NO: 1099597-60-0
• Molecular Formula: C9H8BrF3
• Molecular Weight: 253.0590296
• Mol File: 1099597-60-0.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-Bromo-3-(3,3,3-trifluoropropyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Bromo-3-(3,3,3-trifluoropropyl)benzene(1099597-60-0)
• EPA Substance Registry System: 1-Bromo-3-(3,3,3-trifluoropropyl)benzene(1099597-60-0)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 1099597-60-0(Hazardous Substances Data)

Usage

Structure

Benzene derivative with a bromine atom and a 3,3,3-trifluoropropyl group attached to the benzene ring

Applications

a. Organic synthesis
b. Chemical research
c. Building block for various organic molecules and pharmaceuticals
d. Synthesis of functionalized polymers and materials
e. Production of specialty chemicals and agrochemicals

Safety

Handle with care and follow proper safety procedures due to potential health hazards if not used and stored appropriately.

Upstream product

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Relevant articles and documents

Method for preparing fluoroalkane substituted compound by reducing halogenated fluoroalkane and olefin through metal elementary substance

The invention discloses a method for preparing a fluoroalkane substituted compound, which comprises the steps of taking a compound containing carbon-carbon double bonds and halogenated fluoroalkane as raw materials, taking a metal elementary substance as a reducing agent, taking a substance containing active protons as a hydrogen source, and carrying out an addition reaction to prepare a compound which is simultaneously substituted by hydrogen and fluoroalkyl, thereby obtaining the fluoroalkane substituted compound. According to the method, the metal elementary substance is used as the reducing agent for the first time, the compound containing active hydrogen is used as the hydrogen source, one hydrogen atom and one fluoroalkyl group are introduced to the two ends of olefin respectively, only one-step reaction is needed, the reaction process conditions are mild, the reaction raw materials are cheap and easy to obtain, the cost is low, and all reaction reagents are green and environmentally friendly; and the reaction substrate has strong applicability, can participate in the reaction as long as carbon-carbon double bonds exist in the structure, and is not influenced by the types of substituent groups on carbon atoms of the double bonds, and the yield of the product is good.