Benzyl 2-Bromoethyl Ether TCI B2817

Chemical Identity

CAS No.: 1462-37-9
PubChem: CID 73833·SID 87560439
Formula: C9H11BrO
Molecular weight: 215.09 g/mol
Purity: >97.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-bromoethoxymethylbenzene
SMILES: C1=CC=C(C=C1)COCCBr
InChIKey: FWOHDAGPWDEWIB-UHFFFAOYSA-N

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Benzyl 2-Bromoethyl Ether (BCBE), with CAS number 1462-37-9, is a chemical building block widely used in organic synthesis to create complex molecular structures. As a versatile reagent, it plays a crucial role in laboratories by enabling the formation of new chemical bonds through various reaction mechanisms, including SN2 and electrophilic substitution. Its presence in chemical laboratories is essential for researchers aiming to develop novel compounds, particularly in the field of heterocyclic and branched chain synthesis. Due to its reactivity and structural versatility, BCBE is a key component in many synthetic pathways, making it an indispensable tool for both academic and industrial chemists.

The chemical properties of BCBE make it a preferred choice for synthetic chemists. It exhibits stability under controlled conditions, allowing for predictable reaction outcomes. Its bromoethyl group provides a reactive site that can be modified through various functional group transformations, enhancing its utility in synthetic strategies. The molecule’s ability to participate in multiple reaction types, such as covalent bond formation and substitution reactions, further solidifies its position as a valuable reagent. These characteristics make it ideal for applications requiring controlled reactivity and structural modification.

In Indonesian laboratories, BCBE is commonly used in organic chemistry research and educational settings. It is frequently employed in the synthesis of new compounds, particularly in projects involving heterocyclic and branched chain structures. Additionally, it is utilized in higher education to train students in chemical synthesis techniques and molecular manipulation. Its role in both research and teaching underscores its importance in the chemical sciences within Indonesia.

Related TCI products

Organic synthesis projects benefit from BCBE's ability to form new chemical bonds through SN2 and electrophilic substitution reactions.
Heterocyclic compound development utilizes BCBE's reactive bromoethyl group for structural modification and functional group transformation.
Branched chain synthesis applications take advantage of BCBE's structural versatility to create complex molecular architectures.
Educational institutions use BCBE to teach students about chemical synthesis techniques and molecular manipulation in laboratory settings.
Research laboratories incorporate BCBE into their workflows for the development of novel compounds with specific reactivity and structural features.

Brand	TCI
CAS number	1462-37-9
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Liquid
Storage	Store in a cool, dry place away from light and incompatible materials

BCBE should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and evaporation. Due to its reactive nature, it should be kept separate from strong bases, oxidizing agents, and other incompatible substances. Proper ventilation is essential when handling BCBE to minimize exposure to vapors. Laboratory personnel should wear appropriate personal protective equipment, including gloves, goggles, and a lab coat, to ensure safety during handling and use.

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