114086-15-6 | 2-Methyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$64.00	$45.00
250mg	95%	in stock	$131.00	$92.00
500mg	95%	in stock	$168.00	$118.00
1g	95%	in stock	$173.00	$121.00
5g	95%	in stock	$517.00	$362.00
10g	95%	in stock	$861.00	$603.00

Description

• Catalog Number: AA13441
• Chemical Name: 2-Methyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide
• CAS Number: 114086-15-6
• Molecular Formula: C6H14Br2N2
• Molecular Weight: 273.9968
• MDL Number: MFCD01863510
• SMILES: CN1CC2CC1CN2.Br.Br

Computed Properties

• Complexity: 103
• Covalently-Bonded Unit Count: 3
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 3
• Undefined Atom Stereocenter Count: 2

Upstream Synthesis Route

2-Methyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide is a versatile chemical compound widely used in chemical synthesis applications. This compound serves as an efficient and selective catalyst in a variety of organic transformations due to its unique structure and reactivity. In the realm of chemical synthesis, 2-Methyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide is particularly valued for its ability to facilitate asymmetric reactions, where the formation of chiral molecules with high enantioselectivity is desired. It is commonly employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where stereochemistry plays a crucial role in determining the biological activity or functionality of the end product.Furthermore, this compound's catalytic properties make it a preferred choice in reactions involving imine formation, Michael additions, and various other transformations where the presence of a strong base and nucleophile is essential for driving the desired chemical reactivity. Its stability and ease of handling also make it a practical option for large-scale synthetic processes in the pharmaceutical and chemical industries.Overall, 2-Methyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide stands out as a valuable tool in the hands of synthetic chemists, offering them a reliable and efficient means to access a wide range of complex molecular structures with high levels of control over stereochemistry and product selectivity.