112626-50-3 | 3-Azabicyclo[3.3.0]octane, HCl

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$8.00	$6.00
5g	97%	in stock	$10.00	$7.00
10g	97%	in stock	$12.00	$9.00
25g	97%	in stock	$28.00	$19.00
100g	97%	in stock	$61.00	$43.00
500g	97%	in stock	$302.00	$211.00

Description

• Catalog Number: AB64330
• Chemical Name: 3-Azabicyclo[3.3.0]octane, HCl
• CAS Number: 112626-50-3
• Molecular Formula: C7H14ClN
• Molecular Weight: 147.6458
• MDL Number: MFCD06411019
• SMILES: C1CC2C(C1)CNC2.Cl

Computed Properties

• Complexity: 80.4
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 2
• Undefined Atom Stereocenter Count: 2

Upstream Synthesis Route

3-Azabicyclo[3.3.0]octane hydrochloride, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the production of pharmaceuticals, agrochemicals, and other fine chemicals. With its unique bicyclic structure, 3-Azabicyclo[3.3.0]octane hydrochloride facilitates the synthesis of complex molecules with high efficiency and selectivity.In organic synthesis, 3-Azabicyclo[3.3.0]octane hydrochloride plays a crucial role as a chiral auxiliary, enabling the asymmetric synthesis of various molecules. Its presence in reactions promotes the formation of enantiomerically pure products, making it an essential tool for the production of stereochemically complex compounds.Furthermore, 3-Azabicyclo[3.3.0]octane hydrochloride is utilized in the preparation of heterocyclic compounds and as a key intermediate in the synthesis of bioactive molecules. Its ability to undergo diverse chemical transformations makes it a valuable asset in the development of new pharmaceuticals and organic compounds with enhanced biological activity.Overall, the application of 3-Azabicyclo[3.3.0]octane hydrochloride in chemical synthesis extends across various industries, highlighting its significance in the creation of complex molecules and the advancement of chemical research and development.