201863-99-2

Basic information

• Product Name: (R)-b-AMino-4-chlorobenzenepropanol
• Synonyms: (R)-b-AMino-4-chlorobenzenepropanol;(R)-beta-Amino-4-chlorobenzenepropanol;2(R)-Amino-3-(4-chlorophenyl)propanol;(R)-2-amino-3-(4-chlorophenyl)propan-1-ol;(bR)-b-amino-4-chloro- Benzenepropanol
• CAS NO: 201863-99-2
• Molecular Formula: C₉H₁₂ClNO
• Molecular Weight: 185.65068
• Mol File: 201863-99-2.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (R)-b-AMino-4-chlorobenzenepropanol(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-b-AMino-4-chlorobenzenepropanol(201863-99-2)
• EPA Substance Registry System: (R)-b-AMino-4-chlorobenzenepropanol(201863-99-2)

Safety Data

• Hazardous Substances Data: 201863-99-2(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
(R)-b-AMino-4-chlorobenzenepropanol is used as a building block in organic synthesis for the creation of various chemical compounds. Its unique structure and functional groups make it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Production:
(R)-b-AMino-4-chlorobenzenepropanol is used as a precursor in the production of pharmaceuticals. Its specific stereochemistry and structural characteristics allow it to be a key intermediate in the synthesis of drugs with targeted therapeutic effects.
Used in Chemical Compound Development:
(R)-b-AMino-4-chlorobenzenepropanol is utilized in the development of new chemical compounds with specific properties. Its versatility in chemical reactions and potential to form novel structures make it an important compound in the field of chemical research and development.
Used in Specialty Chemicals Industry:
(R)-b-AMino-4-chlorobenzenepropanol is employed in the specialty chemicals industry for the production of high-value compounds with unique properties. Its specific stereochemistry and reactivity contribute to the creation of specialty chemicals for various applications, such as coatings, adhesives, and polymers.

Upstream product

• 35373-63-8 (R,S)-2-amino-3-p-chlorophenyl-1-propanol 
• 14091-08-8 para-Chloro-D-phenylalanine 

Relevant articles and documents

Electronic effects of aryl-substituted bis(oxazoline) ligands on the outcome of asymmetric copper-catalysed C-H insertion and aromatic addition reactions

The effect of the modification of bis(oxazoline) ligands on the outcome of copper-catalysed C-H insertion and aromatic addition reactions is described. In general, these reactions display minimum sensitivity in terms of enantiocontrol to variation of the electronic properties of the aryl moiety of the ligand however, some influence is observed for C-H insertions employing naphthyl-substituted bis(oxazolines) and for aromatic addition reactions of biphenyl diazo ketone substrates. The synthesis of the modified bis(oxazolines), which include four novel structures, is also described.

COMPOSITIONS AND METHODS FOR CYCLOFRUCTANS AS SEPARATION AGENTS

The present invention relates to derivatized cyclofructan compounds, compositions comprising derivatized cyclofructan compounds, and methods of using compositions comprising derivatized cyclofructan compounds for chromatographic separations of chemical species, including enantiomers. Said compositions may comprise a solid support and/or polymers comprising derivatized cyclofructan compounds.