3-BROMO-1-PROPENE

3-Bromo-1-propene is a reactive halogenated hydrocarbon widely used as an intermediate in organic synthesis and industrial chemical processes.
3-Bromo-1-propene is valued for its ability to introduce allyl functionality into a variety of compounds through substitution and addition reactions.
3-Bromo-1-propene is commonly utilized in pharmaceuticals, agrochemicals, polymers, and research applications.

CAS Number: 106-95-6
EC Number: 203-444-5
Molecular Formula: C3H5Br
Molecular Weight: 120.98 g/mol

Synonyms: Allyl Bromide, 1-Propene, 3-bromo-, 3-Bromopropene, Monobromoallyl, Prop-2-en-1-yl bromide, Bromopropene, Allyl bromide reagent, Allyl bromide for synthesis, 3-Bromoallyl compound, 3‑Bromo‑1‑propene, Allyl bromide, 2‑Propenyl bromide, 3‑Bromopropene, 3‑Bromopropylene, Bromoallylene, 1‑Bromo‑2‑propene, BrCH₂CH=CH₂, Allyl bromide stabilized, AB, C₃H₅Br, CAS 106‑95‑6, PubChem 7841, EC 203‑446‑6, UN 1099, RTECS UC7090000, 3‑Bromoprop‑1-ene, Propene,3-bromo-, Allyl halide, Aliphatic bromide, Alkyl bromide, Organic halide, Electrophilic alkylating agent, Alkylating reagent, Allylating agent, Synthesis intermediate, Polymer precursor, Pharmaceutical intermediate, Perfume intermediate, Agrochemical precursor, Resin intermediate, Allylzinc bromide precursor, Grignard reagent precursor, Electrophile, Lab reagent, Industrial reagent, Volatile alkyl bromide, Irritant bromide

APPLICATIONS

3-Bromo-1-propene is used in organic chemistry for alkylation reactions involving nucleophiles like amines and thiols.
3-Bromo-1-propene serves as a precursor for the synthesis of pharmaceuticals including antiviral and anticancer agents.
3-Bromo-1-propene is involved in the development of bioactive intermediates in medicinal chemistry.

3-Bromo-1-propene is used in agrochemical synthesis to produce herbicides, insecticides, and fungicides.
3-Bromo-1-propene helps form compounds with improved selectivity and biological efficacy in crop protection.
3-Bromo-1-propene is used to introduce functional groups into agrochemical molecules via SN2 mechanisms.

3-Bromo-1-propene is applied in polymer chemistry to functionalize monomers and prepolymers.
3-Bromo-1-propene is used to modify epoxy resins and improve cross-linking in thermoset materials.
3-Bromo-1-propene aids in synthesizing polymers with allyl side chains for enhanced flexibility.

3-Bromo-1-propene is utilized in fragrance and flavor industries for forming allyl esters and ethers.
3-Bromo-1-propene derivatives are used in aroma compound synthesis with fruity, pungent, or spicy notes.
3-Bromo-1-propene provides reactive handles for forming essential oil analogs.

3-Bromo-1-propene is employed in academic research to study transition-metal catalyzed coupling reactions.
3-Bromo-1-propene is a model compound for developing new catalytic strategies involving allyl intermediates.
3-Bromo-1-propene is used in asymmetric synthesis to explore chiral transformations.

3-Bromo-1-propene is used in rubber chemistry for producing vulcanization accelerators and processing aids.
3-Bromo-1-propene improves flexibility and elasticity in elastomers.
3-Bromo-1-propene derivatives enhance the stability and shelf-life of specialty rubbers.

3-Bromo-1-propene is a raw material in the preparation of UV-curable resins and coatings.
3-Bromo-1-propene participates in free-radical polymerization reactions for fast-setting systems.
3-Bromo-1-propene enhances mechanical properties in radiation-cured paints and inks.

3-Bromo-1-propene is used in chemical research for developing new synthetic methodologies.
3-Bromo-1-propene plays a role in carbon–carbon bond formation in organic synthesis.

3-Bromo-1-propene is investigated in flow chemistry and microreactor systems for process intensification.
3-Bromo-1-propene is used as a reactive intermediate in the synthesis of pharmaceuticals.

3-Bromo-1-propene is employed in agrochemical production to introduce allyl functionality.
3-Bromo-1-propene is used in polymer modification to create functionalized polymers.
3-Bromo-1-propene is applied in cross-coupling reactions in organic synthesis.

3-Bromo-1-propene is used in the preparation of biologically active heterocycles.
3-Bromo-1-propene is utilized in the manufacture of specialty monomers.

3-Bromo-1-propene is used to introduce allylic bromides into target molecules.
3-Bromo-1-propene is applied in the synthesis of dyes and pigments.

3-Bromo-1-propene is used in academic laboratories for synthetic chemistry training.
3-Bromo-1-propene is involved in the preparation of surfactants and emulsifiers.
3-Bromo-1-propene is used to synthesize functional alkylated aromatic compounds.

3-Bromo-1-propene is used in organic reactions requiring nucleophilic substitution.
3-Bromo-1-propene is employed in the development of organometallic catalysts.

3-Bromo-1-propene is used to synthesize allylic ethers and alcohols.
3-Bromo-1-propene is a starting material for allylation reactions.

3-Bromo-1-propene is used in the production of fragrance and flavor intermediates.
3-Bromo-1-propene is applied in the synthesis of allylic esters.

3-Bromo-1-propene is used in the development of bioactive molecules.
3-Bromo-1-propene is employed in the design of polymer crosslinkers.

3-Bromo-1-propene is used in multi-step synthesis of pharmaceutical APIs.
3-Bromo-1-propene is used in the synthesis of alkylated nucleosides.

3-Bromo-1-propene is used in studies involving radical chemistry.
3-Bromo-1-propene is used in alkylation of nitrogen-containing heterocycles.

3-Bromo-1-propene is employed in allyl-functionalized silane synthesis.
3-Bromo-1-propene is used to prepare precursors for UV-cured coatings.
3-Bromo-1-propene is utilized in manufacturing epoxy curing agents.

3-Bromo-1-propene is used in photopolymer chemistry.
3-Bromo-1-propene is used to functionalize olefins in material science.

3-Bromo-1-propene is applied in the derivatization of amino acids.
3-Bromo-1-propene is used in the synthesis of alkene-modified cellulose.

3-Bromo-1-propene is employed in allyl-substituted thiol synthesis.
3-Bromo-1-propene is used to prepare complex polycyclic structures.

3-Bromo-1-propene is used in preparing hydrophobic monomer intermediates.
3-Bromo-1-propene is involved in formation of metal-allyl complexes.

3-Bromo-1-propene is applied in asymmetric synthesis protocols.
3-Bromo-1-propene is used in C–C bond forming reactions.

3-Bromo-1-propene is used to modify the backbones of natural products.
3-Bromo-1-propene is used in functionalization of oleochemical derivatives.

3-Bromo-1-propene is applied in enzyme inhibitor research.
3-Bromo-1-propene is used to prepare allyl-functional polymers for adhesives.
3-Bromo-1-propene is used in the production of reactive coating additives.

3-Bromo-1-propene is utilized in synthesis of alkene-containing ketones.
3-Bromo-1-propene is used to synthesize allyl sulfonates.

3-Bromo-1-propene is used to prepare anti-microbial candidate molecules.
3-Bromo-1-propene is employed in allyl aryl ether synthesis.
3-Bromo-1-propene is used in development of modified peptide backbones.

3-Bromo-1-propene is applied in allyl substitution for organosilicon chemistry.
3-Bromo-1-propene is used in ring-closing metathesis applications.

3-Bromo-1-propene is used in the synthesis of allylic halide derivatives for further transformation.
3-Bromo-1-propene is used in creating intermediates for liquid crystal materials.

DESCRIPTION

3-Bromo-1-propene is a volatile, colorless to pale yellow liquid with a sharp, pungent odor.
It consists of a three-carbon chain with a double bond between C2 and C3 and a bromine atom on the C1 position.
3-Bromo-1-propene is flammable and highly reactive, especially under heat and light.

3-Bromo-1-propene is prone to polymerization and should be stabilized during storage.
It is immiscible with water but dissolves in common organic solvents like ether, benzene, and alcohol.
3-Bromo-1-propene is sensitive to moisture and light and may release fumes when heated.

3-Bromo-1-propene is a lachrymator and can cause irritation to eyes, skin, and respiratory tract.
It should be handled in well-ventilated environments using proper personal protective equipment.
Despite its hazards, 3-Bromo-1-propene is a highly useful reagent due to its reactivity and versatility.

3-Bromo-1-propene is regulated due to its toxicological profile and flammability.
It is used under controlled conditions in laboratories and industrial facilities.
3-Bromo-1-propene remains a crucial intermediate in synthetic chemistry.

3-Bromo-1-propene is an organobromine compound with the molecular formula C3H5Br.
3-Bromo-1-propene is a clear, colorless to pale yellow liquid with a strong, irritating odor.
3-Bromo-1-propene is classified as an allyl halide, combining alkene and halogen reactivity.

3-Bromo-1-propene is highly reactive in nucleophilic substitution and elimination reactions.
3-Bromo-1-propene is flammable and volatile, requiring careful storage and handling.

3-Bromo-1-propene is typically stored in tightly sealed containers under cool, dry conditions.
3-Bromo-1-propene has both industrial and academic importance in synthetic chemistry.

PROPERTIES

Chemical Formula: C3H5Br
Molecular Weight: 120.98 g/mol
Appearance: Colorless to light yellow liquid
Odor: Sharp, pungent
Density: ~1.398 g/cm³ at 20°C
Melting Point: −119°C
Boiling Point: ~71°C
Flash Point: −5°C (closed cup)
Solubility: Insoluble in water; soluble in organic solvents
Vapor Pressure: ~86 mmHg at 25°C
Reactivity: Highly reactive with nucleophiles; sensitive to light and heat
Stability: May polymerize; requires stabilization
Storage Conditions: Cool, dry, dark environment in sealed containers
Hazards: Flammable, toxic, irritant, lachrymator

FIRST AID

Inhalation:
Move person to fresh air immediately.
Administer oxygen or artificial respiration if needed.
Seek emergency medical assistance for respiratory symptoms.

Skin Contact:
Remove contaminated clothing.
Wash skin thoroughly with soap and water.
Seek medical advice if irritation persists.

Eye Contact:
Rinse eyes with clean water for 15 minutes while holding eyelids apart.
Remove contact lenses if possible.
Seek urgent medical evaluation.

Ingestion:
Do not induce vomiting.
Rinse mouth and give small amounts of water if conscious.
Seek immediate medical attention.

Note to Physicians:
Treat symptomatically.
Monitor for respiratory distress and provide supportive care.
Consider activated charcoal if ingestion is recent and the patient is conscious.

HANDLING AND STORAGE

Handling:
Use in well-ventilated areas or fume hoods.
Avoid breathing vapors and avoid all contact with skin and eyes.
Wear gloves, goggles, and chemical-resistant clothing.
Do not smoke, eat, or drink while handling.

Storage:
Keep container tightly closed in a cool, dry, well-ventilated place.
Protect from heat, direct sunlight, and ignition sources.
Use stabilizers to inhibit polymerization if required.
Store away from oxidizers and bases.

Spill Response:
Evacuate and ventilate area.
Use absorbent materials (e.g., vermiculite) to contain spill.
Dispose of materials according to hazardous waste regulations.

Disposal:
Dispose of through a licensed chemical waste disposal contractor.
Do not allow release into drains or the environment.