759-97-7 | 2-Bromo-1,1,3-trimethoxypropane

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$36.00	$25.00
5g	97%	in stock	$100.00	$70.00
10g	97%	in stock	$176.00	$123.00
25g	97%	in stock	$348.00	$243.00

Description

• Catalog Number: AB48201
• Chemical Name: 2-Bromo-1,1,3-trimethoxypropane
• CAS Number: 759-97-7
• Molecular Formula: C6H13BrO3
• Molecular Weight: 213.0696
• MDL Number: MFCD00191863
• SMILES: COCC(C(OC)OC)Br
• NSC Number: 6388

Computed Properties

• Complexity: 75.4
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 5
• Undefined Atom Stereocenter Count: 1
• XLogP3: 0.8

Upstream Synthesis Route

2-Bromo-1,1,3-trimethoxypropane is a versatile compound widely utilized in chemical synthesis due to its unique reactivity and structural properties. This compound serves as a key intermediate in the synthesis of various organic molecules, particularly in the preparation of diverse functionalized organic compounds.One of the primary applications of 2-Bromo-1,1,3-trimethoxypropane is in the synthesis of pharmaceutical intermediates, where it is employed as a key building block in the assembly of complex drug molecules. Its reactivity allows for the introduction of functional groups at specific positions, enabling chemists to tailor the properties of the final compounds. Additionally, this compound is utilized in the preparation of agrochemicals, specialty chemicals, and materials with specific properties.In chemical synthesis, 2-Bromo-1,1,3-trimethoxypropane acts as a valuable reagent in various transformations such as nucleophilic substitution reactions and coupling reactions. Its unique structure facilitates selective reactions and enables the formation of intricate molecular architectures. Furthermore, this compound can participate in cascade reactions, leading to the rapid generation of structurally diverse compounds in a single synthetic step.Overall, the application of 2-Bromo-1,1,3-trimethoxypropane in chemical synthesis offers chemists a powerful tool for the efficient construction of complex molecules with precise control over functionality and stereochemistry. Its versatility and reactivity make it an essential component in the toolbox of synthetic chemists seeking to access new and challenging molecular targets.

Literature

• Selective sensing of Cu(II) at ng ml(-1) level based on phosphorescence quenching of 1-bromo-2-methylnaphthalene sandwiched in sodium deoxycholate dimer.

  Chemical communications (Cambridge, England) 20050227