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3,3-Dimethylallyl bromide
[CAS# 870-63-3]

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Complete supplier list of 3,3-Dimethylallyl bromide
Identification
Classification Organic raw materials >> Hydrocarbon compounds and their derivatives >> Hydrocarbon halide
Name 3,3-Dimethylallyl bromide
Synonyms 1-Bromo-3-methyl-2-butene; 4-Bromo-2-methyl-2-butene; Prenyl bromide
Molecular Structure CAS # 870-63-3, 3,3-Dimethylallyl bromide, 1-Bromo-3-methyl-2-butene, 4-Bromo-2-methyl-2-butene, Prenyl bromide
Molecular Formula C5H9Br
Molecular Weight 149.03
CAS Registry Number 870-63-3
EC Number 212-799-5
SMILES CC(=CCBr)C
Properties
Density 1.27
Boiling point 82-83 ºC (150 mmHg)
Refractive index 1.489-1.491
Flash point 32 ºC
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319-H335    Details
Precautionary Statements P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Specific target organ toxicity - single exposureSTOT SE3H335
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Skin corrosionSkin Corr.1BH314
Flammable liquidsFlam. Liq.3H226
Serious eye damageEye Dam.1H318
Acute toxicityAcute Tox.4H301
Acute hazardous to the aquatic environmentAquatic Acute1H400
Acute toxicityAcute Tox.3H330
Transport Information UN 2920
SDS Available
up Discovory and Applicatios
3,3-Dimethylallyl bromide, a chemical compound with the molecular formula C6H11Br, was first synthesized in the early 20th century as part of the exploration of organic synthesis and chemical reactivity. This compound was discovered through the bromination of dimethylallyl alcohol, resulting in the formation of a bromoalkene derivative. The discovery of 3,3-dimethylallyl bromide contributed to the development of organic chemistry by expanding the repertoire of available chemical reactions and functional group transformations.

3,3-Dimethylallyl bromide is commonly used as an allylating agent in organic synthesis. It reacts with nucleophiles, such as carbon, oxygen, nitrogen, and sulfur-containing compounds, to introduce the allyl group. This allylation reaction is valuable in creating carbon-carbon and carbon-heteroatom bonds, leading to the synthesis of complex organic molecules.

The allylation capability of 3,3-dimethylallyl bromide is particularly useful in the synthesis of natural products and pharmaceutical intermediates. It serves as a key building block for constructing complex molecular frameworks found in natural products with biological activity. By incorporating the allyl group into target molecules, chemists can access diverse chemical structures with potential medicinal properties.

3,3-Dimethylallyl bromide is employed in organometallic chemistry as a ligand precursor for transition metal catalysts. Coordination of the allyl group to metal centers enables catalytic transformations such as allylic substitutions, cross-coupling reactions, and cyclizations. These reactions are essential in synthetic chemistry for creating carbon-carbon bonds and functionalizing organic molecules with high efficiency and selectivity.

In polymer chemistry, 3,3-dimethylallyl bromide is utilized as a monomer for the synthesis of allyl-containing polymers. Through polymerization reactions, it can be incorporated into polymer chains to impart specific properties, such as flexibility, adhesion, or thermal stability. Allyl-containing polymers find applications in industries such as adhesives, coatings, and materials science.

3,3-Dimethylallyl bromide derivatives have potential applications in medicinal chemistry. By modifying the allyl group or incorporating it into bioactive molecules, researchers can create compounds with enhanced pharmacological properties. These compounds may exhibit activities such as anticancer, antimicrobial, or anti-inflammatory effects, making them promising candidates for drug discovery and development.

Allyl-containing compounds, including those derived from 3,3-dimethylallyl bromide, are utilized in the flavor and fragrance industry. They contribute to the aroma and taste profiles of various food products, beverages, perfumes, and cosmetics. The allyl group imparts characteristic notes, such as floral, fruity, or spicy, enhancing the sensory experience of consumer goods.
Market Analysis Reports
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