1233501-44-4 Usage
Uses
Used in Pharmaceutical Industry:
(R)-3-CHLORO-1-(3,4-DICHLORO-PHENYL)-PROPAN-1-OL is used as an intermediate in the synthesis of various pharmaceuticals. Its unique structure and reactivity contribute to the development of new drugs and medications, playing a crucial role in advancing medical treatments.
Used in Agrochemical Industry:
In the agrochemical sector, (R)-3-CHLORO-1-(3,4-DICHLORO-PHENYL)-PROPAN-1-OL serves as an intermediate for the production of different agrochemicals. Its properties make it suitable for the creation of compounds that can be used in agriculture to improve crop protection and yield.
Used in Research and Development:
(R)-3-CHLORO-1-(3,4-DICHLORO-PHENYL)-PROPAN-1-OL is also utilized in research and development, where it acts as a key component in the synthesis of complex molecules. Its potential applications in organic chemistry make it an essential building block for creating novel compounds with various functions and properties.
Used in Organic Chemistry:
As a building block in organic chemistry, (R)-3-CHLORO-1-(3,4-DICHLORO-PHENYL)-PROPAN-1-OL is used for the synthesis of more complex molecules. Its unique structure and reactivity allow chemists to explore new pathways and create innovative compounds with potential applications in various fields, including materials science, pharmaceuticals, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 1233501-44-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,3,5,0 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1233501-44:
(9*1)+(8*2)+(7*3)+(6*3)+(5*5)+(4*0)+(3*1)+(2*4)+(1*4)=104
104 % 10 = 4
So 1233501-44-4 is a valid CAS Registry Number.
1233501-44-4Relevant academic research and scientific papers
De Angelis, Sonia,De Renzo, Maddalena,Carlucci, Claudia,Degennaro, Leonardo,Luisi, Renzo
, p. 4304 - 4311 (2016)
A convenient, versatile, and green CBS-asymmetric reduction of aryl and heteroaryl ketones has been developed by using the microreactor technology. The study demonstrates that it is possible to handle borane solution safely within microreactors and that the reaction performs well using 2-MeTHF as a greener solvent.
