1951425-23-2 | (2S)-2-Amino-2-(3-fluoro-2-methylphenyl)ethan-1-ol hcl

Packsize	Purity	Availability	Price	Discounted Price
1mg	95%	2 weeks	$284.00	$199.00
5mg	95%	2 weeks	$303.00	$212.00
10mg	95%	2 weeks	$338.00	$237.00
1g	95%	2 weeks	$1,452.00	$1,016.00

Description

• Catalog Number: AI43649
• Chemical Name: (2S)-2-Amino-2-(3-fluoro-2-methylphenyl)ethan-1-ol hcl
• CAS Number: 1951425-23-2
• Molecular Formula: C9H13ClFNO
• Molecular Weight: 205.657
• MDL Number: MFCD24417001
• SMILES: Cc1c([C@@H](CO)N)cccc1F.Cl

Computed Properties

• Complexity: 143
• Covalently-Bonded Unit Count: 2
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 3
• Rotatable Bond Count: 2

Upstream Synthesis Route

(S)-2-Amino-2-(3-fluoro-2-methylphenyl)ethanol hydrochloride is a versatile chemical compound that finds widespread application in chemical synthesis. This compound serves as a chiral building block in organic chemistry, particularly in the preparation of enantiopure compounds. Due to its unique stereochemical properties, (S)-2-Amino-2-(3-fluoro-2-methylphenyl)ethanol hydrochloride is utilized in the asymmetric synthesis of pharmaceuticals, agrochemicals, and fine chemicals.One of the key applications of (S)-2-Amino-2-(3-fluoro-2-methylphenyl)ethanol hydrochloride is in the development of chiral ligands for catalytic reactions. This compound can act as a ligand in transition metal-catalyzed reactions, enabling the selective formation of chiral products. By incorporating (S)-2-Amino-2-(3-fluoro-2-methylphenyl)ethanol hydrochloride into the reaction system, chemists can control the stereochemistry of the final product, enhancing the efficiency and selectivity of the synthesis process.Furthermore, (S)-2-Amino-2-(3-fluoro-2-methylphenyl)ethanol hydrochloride can be used in the synthesis of complex molecules with defined stereochemistry. Its presence in the reaction mixture can influence the direction of asymmetric transformations, leading to the formation of enantiomerically pure compounds. This is particularly valuable in the pharmaceutical industry, where the chirality of a molecule can significantly impact its biological activity and pharmacological properties.In summary, (S)-2-Amino-2-(3-fluoro-2-methylphenyl)ethanol hydrochloride plays a crucial role in chemical synthesis by serving as a chiral auxiliary, ligand, or building block for the preparation of enantiomerically enriched compounds. Its versatile applications in asymmetric synthesis make it a valuable tool for organic chemists seeking to access complex molecules with high stereochemical purity.