925430-39-3

Usage

Uses

Used in Pharmaceutical Industry:
(R)-2-chloro-1-(3-hydroxyphenyl)ethanol is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and functional groups allow for the development of drugs targeting a range of diseases, making it a valuable asset in the industry.
Used in Agrochemical Industry:
In the agrochemical sector, (R)-2-chloro-1-(3-hydroxyphenyl)ethanol serves as a key component in the synthesis of compounds with potential applications in agriculture, such as pesticides and other chemical products designed to enhance crop protection and yield.
Used in Medicinal Chemistry Research and Development:
(R)-2-chloro-1-(3-hydroxyphenyl)ethanol is utilized as a promising candidate for further research and development in medicinal chemistry. Its biological activity and pharmacological properties make it an attractive option for exploring new therapeutic approaches and advancing the understanding of its potential applications in treating various diseases.

Upstream product

• 62932-90-5 2-chloro-1-(3-hydroxy phenyl)ethan-1-one 
• 121-71-1 3-Hydroxyacetophenone 

Downstream Products

• 925430-42-8 3-(2-azido-1-hydroxy-ethyl)-phenol 
• 61-76-7 phenylephrine hydrochloride 
• 5596-07-6 (+)-Norphenylephrine 

Relevant academic research and scientific papers

Preparation method of L-phenylephrine hydrochloride

The invention relates to a preparation method of L-phenylephrine hydrochloride, and specifically discloses a preparation method of L-phenylephrine hydrochloride, which comprises the steps of chlorination reaction, chiral reduction reaction, amination salifying and recrystallization. The preparation method has the advantages of cheap and easily available raw materials, simple operation process, loweconomic cost, high product yield and the like, and the product quality meets the standard requirements of Chinese Pharmacopoeia and European Pharmacopoeia.

Asymmetric hydrogenation of α-chloro aromatic ketones catalyzed by η6-arene/TsDPEN-ruthenium(II) complexes

(Chemical Equation Presented) Asymmetric hydrogenation of various α-chloro aromatic ketones with Ru(OTf)(TsDPEN)(η6-arene) (TsDPEN = N-(p-toluenesulfonyl)-1,2-diphenylethylenediamine) produces the chiral chlorohydrins in up to 98% ee. This reac

Practical synthesis of optically active styrene oxides via reductive transformation of 2-chloroacetophenones with chiral rhodium catalysts

(equation presented) A practical method for the synthesis of optically active styrene oxides has been developed via formation of optically active 2-chloro-1-phenylethanols generated by reductive transformation of ring-substituted 2-chloroacetophenones. Th