24152-71-4 Usage
Physical state
Colorless liquid The compound appears as a colorless liquid, which indicates its lack of color and its ability to flow.
Uses as an intermediate
Synthesis of pharmaceuticals and agrochemicals 1-methoxy-3-phenylamino-propan-2-ol is often used as a starting material or intermediate in the production of various drugs and chemicals used in agriculture.
Building block in production
Dyes and pigments The compound serves as a fundamental component in the creation of various dyes and pigments, which can be used in a wide range of industries, including textiles, paints, and plastics.
Medicinal properties
Anti-inflammatory and analgesic effects 1-methoxy-3-phenylamino-propan-2-ol has been found to exhibit properties that can help reduce inflammation and alleviate pain, making it a potential candidate for drug development in these areas.
Versatility
Used in various industries The compound's diverse applications across different industries, such as pharmaceuticals, agrochemicals, and dyes and pigments, demonstrate its versatility and value as a chemical building block.
Check Digit Verification of cas no
The CAS Registry Mumber 24152-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,1,5 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 24152-71:
(7*2)+(6*4)+(5*1)+(4*5)+(3*2)+(2*7)+(1*1)=84
84 % 10 = 4
So 24152-71-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO2/c1-13-8-10(12)7-11-9-5-3-2-4-6-9/h2-6,10-12H,7-8H2,1H3/t10-/m1/s1
24152-71-4Relevant articles and documents
A Multicomponent Approach to Oxazolidinone Synthesis Catalyzed by Rare-Earth Metal Amides
Zhou, Meixia,Zheng, Xizhou,Wang, Yaorong,Yuan, Dan,Yao, Yingming
, p. 5783 - 5787 (2019/04/14)
Three-component reaction of epoxides, amines, and dimethyl carbonate catalyzed by rare-earth metal amides has been developed to synthesize oxazolidinones. 47 examples of 3,5-disubstituted oxazolidinones were prepared in 13–97 % yields. This is a simple and most practical method which employs easily available substrates and catalysts, and is applicable to a wide range of aromatic and aliphatic amines, as well as mono-substituted epoxides. Scope of disubstituted epoxides is rather limited, which requires further study. Preliminary mechanistic study reveals two possible reaction pathways through intermediates of β-amino alcohols or amides.
