3906-16-9 | (R)-(+)-1-(2-Naphthyl)ethylamine

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$26.00	$18.00
5g	98%	in stock	$36.00	$25.00
10g	98%	in stock	$43.00	$30.00
25g	98%	in stock	$107.00	$75.00
100g	98%	in stock	$425.00	$298.00

Description

• Catalog Number: AB55475
• Chemical Name: (R)-(+)-1-(2-Naphthyl)ethylamine
• CAS Number: 3906-16-9
• Molecular Formula: C12H13N
• Molecular Weight: 171.2383
• MDL Number: MFCD00085367
• SMILES: C[C@H](c1ccc2c(c1)cccc2)N

Computed Properties

• Complexity: 167
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 2.8

Upstream Synthesis Route

As a professional chemist, I can explain the application of (R)-(+)-1-(2-Naphthyl)ethylamine in chemical synthesis. This compound, also known as R-naphthyl ethylamine, is a chiral amine with a naphthyl group attached to an ethylamine backbone. Its specific stereochemistry, denoted by the R configuration, makes it valuable in asymmetric synthesis for producing enantiomerically pure compounds.In chemical synthesis, (R)-(+)-1-(2-Naphthyl)ethylamine serves as a versatile chiral building block for creating pharmaceutically active molecules, agrochemicals, and advanced materials. Its chiral nature allows it to induce asymmetry in reactions, enabling the synthesis of single enantiomers with high optical purity. This compound can be used in various transformations such as asymmetric catalysis, enantioselective reductions, and carbon-carbon bond formations.By utilizing (R)-(+)-1-(2-Naphthyl)ethylamine in chemical synthesis, researchers can control the stereochemistry of the products, leading to enhanced biological activity, improved selectivity, and reduced side effects in drug development. Its application extends to the preparation of chiral ligands, organocatalysts, and chiral auxiliaries, contributing to the advancement of asymmetric synthesis methodologies.Furthermore, the unique structural features of R-naphthyl ethylamine make it a valuable tool in the design of novel molecules for various industries, including pharmaceuticals, agrochemicals, and materials science. Its ability to participate in diverse reactions while maintaining chirality underscores its significance in modern organic chemistry research and development.