116258-17-4 | (1S,4S)-(+)-2-Benzyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$68.00	$48.00
2500mg	95%	in stock	$80.00	$56.00
5g	95%	in stock	$119.00	$84.00
10g	95%	in stock	$238.00	$167.00
25g	95%	in stock	$577.00	$404.00
50g	95%	in stock	$923.00	$647.00

Description

• Catalog Number: AA15419
• Chemical Name: (1S,4S)-(+)-2-Benzyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide
• CAS Number: 116258-17-4
• Molecular Formula: C12H18Br2N2
• Molecular Weight: 350.0927
• MDL Number: MFCD08669797
• SMILES: c1ccc(cc1)CN1C[C@@H]2C[C@H]1CN2.Br.Br

Computed Properties

• Complexity: 199
• Covalently-Bonded Unit Count: 3
• Defined Atom Stereocenter Count: 2
• Heavy Atom Count: 16
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 2

Upstream Synthesis Route

The (1S,4S)-2-Benzyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide is a versatile compound widely used in chemical synthesis as a chiral catalyst. It plays a crucial role in promoting various asymmetric reactions by facilitating the formation of enantiopure products. This compound is particularly effective in catalyzing reactions such as asymmetric Diels-Alder reactions, Michael additions, and aldol reactions, where control over the stereochemistry of the products is essential.Additionally, (1S,4S)-2-Benzyl-2,5-diazabicyclo[2.2.1]heptane dihydrobromide has found applications in the pharmaceutical industry for the synthesis of chiral drug molecules. Its ability to induce chirality in organic molecules makes it a valuable tool for the preparation of biologically active compounds with high optical purity.Overall, this compound is highly sought after in chemical synthesis for its unique chiral properties and its significant impact on controlling stereoselectivity in a variety of reactions. Its use continues to expand in the field of organic chemistry, providing researchers with a powerful tool for achieving efficient and selective synthesis of complex molecules.