59032-45-0

Basic information

• Product Name: 1-Butene, 2-(broMoMethyl)-
• Synonyms: 1-Butene, 2-(broMoMethyl)-
• CAS NO: 59032-45-0
• Molecular Formula: C₅H₉Br
• Molecular Weight: 149.02896
• Mol File: 59032-45-0.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 122.9±9.0 °C(Predicted)
• Appearance: /
• Density: 1.250±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1-Butene, 2-(broMoMethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Butene, 2-(broMoMethyl)-(59032-45-0)
• EPA Substance Registry System: 1-Butene, 2-(broMoMethyl)-(59032-45-0)

Safety Data

• Hazardous Substances Data: 59032-45-0(Hazardous Substances Data)

Usage

Physical State

Colorless liquid

Explanation

The compound is in a liquid state at room temperature and is colorless, meaning it does not have any visible color.

Explanation

The compound has a pleasant, sweet smell when in its liquid form.

Explanation

1-Butene, 2-(bromomethyl)is used as a starting material in the synthesis of various polymers and plastics, which are then used in a wide range of applications.

Explanation

This is another name for the compound, which is used to describe its structure more explicitly.

Explanation

As a monomer, 1-Butene, 2-(bromomethyl)can be polymerized to form larger molecules, which are then used to create resins and synthetic rubbers.

Explanation

The compound can undergo chemical reactions with other substances, resulting in the formation of different products such as 1,4-Dibromobutane and 4-bromo-1-butene.

Explanation

Due to its flammability, 1-Butene, 2-(bromomethyl)poses a fire hazard and should be handled with care to prevent ignition.

Explanation

Ingestion or inhalation of the compound can lead to adverse health effects, and it is important to follow safety protocols when handling this chemical.

Odor

Sweet

Common Uses

Production of polymers and plastics

Role in Manufacturing

Monomer in the production of resins and synthetic rubbers

Chemical Reactions

Can react with other chemicals to form 1,4-Dibromobutane and 4-bromo-1-butene

Safety Classification

Flammable liquid

Hazardous Effects

Harmful if swallowed or inhaled

Upstream product

• 563-46-2 2-Methyl-1-butene 
• 922-63-4 ethylacrolein 
• 4435-54-5 2-Methylene-1-butanol 

Downstream Products

• 1601489-99-9 2-bromo-4-fluoro-N-(4-methoxybenzyl)-N-(2-methylenebutyl)benzenesulfonamide 
• 1601490-06-5 2-bromo-4-fluoro-N-(2-methylenebutyl)benzenesulfonamide 
• 130012-75-8 2-Methylenebutyl Phenyl Ketone 

Relevant articles and documents

Experimental and Computational Studies of Palladium-Catalyzed Spirocyclization via a Narasaka-Heck/C(sp3or sp2)-H Activation Cascade Reaction

The first synthesis of highly strained spirocyclobutane-pyrrolines via a palladium-catalyzed tandem Narasaka-Heck/C(sp3 or sp2)-H activation reaction is reported here. The key step in this transformation is the activation of a δ-C-H bond via an in situ generated σ-alkyl-Pd(II) species to form a five-membered spiro-palladacycle intermediate. The concerted metalation-deprotonation (CMD) process, rate-determining step, and energy barrier of the entire reaction were explored by density functional theory (DFT) calculations. Moreover, a series of control experiments was conducted to probe the rate-determining step and reversibility of the C(sp3)-H activation step.

TRICYCLIC HETEROCYCLE COMPOUNDS USEFUL AS HIV INTEGRASE INHIBITORS

The present invention relates to Tricyclic Heterocycle Compounds of Formula (I): (I) and pharmaceutically acceptable salts or prodrug thereof, wherein R1, R2, R3, R4, R5, R6 and n are as defined herein. The present invention also relates to compositions comprising at least one Tricyclic Heterocycle Compound, and methods of using the Tricyclic Heterocycle Compounds for treating or preventing HIV infection in a subject.

Organic base-catalysed solvent-tuned chemoselective carbotrifluoromethylation and oxytrifluoromethylation of unactivated alkenes

An unprecedented and efficient organic base-catalysed highly chemoselective carbo- and oxytrifluoromethylation of unactivated alkenes with Togni's reagent was developed. The switchable chemoselectivity was tuned by simply changing the organic base catalyst and solvent. Mechanistic studies indicated that a radical cyclization pathway for carbotrifluoromethylation in DMSO and a carbocation pathway for oxytrifluoromethylation in DCE were probably involved.