54149-17-6 | 1-Bromo-2-(2-methoxyethoxy)ethane

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$13.00	$9.00
5g	95%	in stock	$18.00	$13.00
10g	95%	in stock	$30.00	$21.00
25g	95%	in stock	$56.00	$39.00
500g	95%	in stock	$1,008.00	$706.00

Description

• Catalog Number: AB43267
• Chemical Name: 1-Bromo-2-(2-methoxyethoxy)ethane
• CAS Number: 54149-17-6
• Molecular Formula: C5H11BrO2
• Molecular Weight: 183.0436
• MDL Number: MFCD00000238
• SMILES: COCCOCCBr

Computed Properties

• Complexity: 41.4
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 5
• XLogP3: 0.5

Upstream Synthesis Route

1-Bromo-2-(2-methoxyethoxy)ethane, also known as bromoethylene glycol ether, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role as a reagent in various organic reactions due to its unique chemical properties. In chemical synthesis, 1-Bromo-2-(2-methoxyethoxy)ethane is commonly utilized as a versatile alkylating agent. Its bromo functional group allows for efficient coupling reactions with a wide range of nucleophiles, enabling the formation of new carbon-carbon and carbon-oxygen bonds. This compound is particularly valuable in the synthesis of complex organic molecules, such as pharmaceuticals, agrochemicals, and specialty chemicals.Furthermore, the presence of the methoxyethoxy group in 1-Bromo-2-(2-methoxyethoxy)ethane enhances its reactivity and selectivity in various transformations. This functional group can act as a directing agent in certain reactions, facilitating regioselective and stereoselective processes. Additionally, the ether linkage provides stability and solubility to the molecule, making it compatible with a wide range of solvents and reaction conditions.Overall, 1-Bromo-2-(2-methoxyethoxy)ethane is a valuable tool in the arsenal of synthetic chemists, enabling the construction of complex molecular architectures with precision and efficiency. Its versatility and reactivity make it a valuable component in the toolbox of researchers and industrial chemists alike, driving innovation and progress in the field of chemical synthesis.

Literature

• Amine-reactive fluorene probes: synthesis, optical characterization, bioconjugation, and two-photon fluorescence imaging.

  Bioconjugate chemistry 20081217