1147883-41-7

Basic information

• Product Name: (2S)-2-AMINO-2-(4-CHLOROPHENYL)ETHANOL HCL
• Synonyms: (2S)-2-AMINO-2-(4-CHLOROPHENYL)ETHANOL HCL;(2S)-2-amino-2-(4-chlorophenyl)ethanol hydrochloride;(2S)-2-AMINO-2-(4-CHLOROPHENYL)ETHAN-1-OL HCL
• CAS NO: 1147883-41-7
• Molecular Formula: C₈H₁₀ClNO*ClH
• Molecular Weight: 208.08504
• Mol File: 1147883-41-7.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: (2S)-2-AMINO-2-(4-CHLOROPHENYL)ETHANOL HCL(CAS DataBase Reference)
• NIST Chemistry Reference: (2S)-2-AMINO-2-(4-CHLOROPHENYL)ETHANOL HCL(1147883-41-7)
• EPA Substance Registry System: (2S)-2-AMINO-2-(4-CHLOROPHENYL)ETHANOL HCL(1147883-41-7)

Safety Data

• Hazardous Substances Data: 1147883-41-7(Hazardous Substances Data)

Usage

Description

(2S)-2-AMINO-2-(4-CHLOROPHENYL)ETHANOL HCL is a chiral amino alcohol compound, characterized by its white to off-white crystalline powder form. With a molecular formula of C8H11ClNO and a molecular weight of 171.63 g/mol, this compound is soluble in water and ethanol. It is widely recognized for its utility as a chiral building block in the pharmaceutical industry, playing a crucial role in the synthesis of drugs and pharmaceutical intermediates. Moreover, it holds promise in the development of chiral ligands and catalysts for asymmetric synthesis, thereby expanding its applications in the realm of chemistry and drug discovery.

Uses

Used in Pharmaceutical Industry:
(2S)-2-AMINO-2-(4-CHLOROPHENYL)ETHANOL HCL serves as a vital chiral building block for the synthesis of various drugs and pharmaceutical intermediates. Its unique stereochemistry allows for the creation of enantiomerically pure compounds, which is essential for ensuring the desired therapeutic effects and minimizing potential side effects.
Used in Chiral Ligand and Catalyst Preparation:
In the field of asymmetric synthesis, (2S)-2-AMINO-2-(4-CHLOROPHENYL)ETHANOL HCL is utilized in the preparation of chiral ligands and catalysts. These are indispensable for facilitating enantioselective reactions, leading to the production of biologically active compounds with high enantiomeric purity, which is crucial for the development of effective and safe pharmaceuticals.
Safety and Handling:
Given its potential health hazards, (2S)-2-AMINO-2-(4-CHLOROPHENYL)ETHANOL HCL is typically handled and stored in accordance with good laboratory practices and safety guidelines. This ensures the protection of both the environment and the individuals working with this compound, minimizing the risk of exposure and adverse effects.

Downstream Products

• 1426928-72-4 C₂₂H₁₇ClN₄O₂ 
• 1147391-29-4 (S)-4-(4-chlorophenyl)oxazolidin-2-one