Welcome to LookChem.com Sign In|Join Free
  • or
(1R)-2,2,2-TRIFLUORO-1-(3-METHOXYPHENYL)ETHYLAMINE, also known as (R)-(+)-3-Amino-1-(3-methoxyphenyl)-2-propanol, is a chiral amine compound with a unique structure and properties. It is characterized by the presence of a trifluoromethyl group, a chiral center, and a methoxyphenyl group. (1R)-2,2,2-TRIFLUORO-1-(3-METHOXYPHENYL)ETHYLAMINE is important in the pharmaceutical industry due to its potential as a building block for the creation of new drugs and its ability to impart chirality to drug molecules. Additionally, it is used in the synthesis of agrochemicals and the production of chiral ligands for catalysis. Its unique structure and properties make it an important tool in the field of organic chemistry, particularly in the development of asymmetrical synthesis methods.

1213162-90-3

Post Buying Request

1213162-90-3 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

1213162-90-3 Usage

Uses

Used in Pharmaceutical Industry:
(1R)-2,2,2-TRIFLUORO-1-(3-METHOXYPHENYL)ETHYLAMINE is used as a building block for the creation of new drugs. Its chiral nature allows for the development of enantiomerically pure compounds, which can exhibit different biological activities and reduce potential side effects. (1R)-2,2,2-TRIFLUORO-1-(3-METHOXYPHENYL)ETHYLAMINE is particularly useful in the synthesis of chiral pharmaceuticals, where the stereochemistry of the molecule can significantly impact its efficacy and safety.
Used in Agrochemical Industry:
(1R)-2,2,2-TRIFLUORO-1-(3-METHOXYPHENYL)ETHYLAMINE is used in the synthesis of agrochemicals, such as pesticides and herbicides. Its chiral properties enable the development of more effective and selective agrochemicals, reducing the environmental impact and improving crop protection.
Used in Chiral Ligand Production:
(1R)-2,2,2-TRIFLUORO-1-(3-METHOXYPHENYL)ETHYLAMINE is used in the production of chiral ligands for catalysis. These ligands are essential in asymmetric synthesis, allowing for the selective formation of enantiomerically pure compounds. The use of chiral ligands can improve the efficiency and selectivity of catalytic reactions, leading to the production of high-quality chemical products.
Used in Organic Chemistry Research:
(1R)-2,2,2-TRIFLUORO-1-(3-METHOXYPHENYL)ETHYLAMINE is an important tool in the field of organic chemistry, particularly in the development of asymmetrical synthesis methods. Its unique structure and properties make it a valuable compound for studying and understanding the mechanisms of enantioselective reactions. This knowledge can be applied to the design and synthesis of new chiral compounds with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 1213162-90-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,3,1,6 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1213162-90:
(9*1)+(8*2)+(7*1)+(6*3)+(5*1)+(4*6)+(3*2)+(2*9)+(1*0)=103
103 % 10 = 3
So 1213162-90-3 is a valid CAS Registry Number.

1213162-90-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R)-2,2,2-trifluoro-1-(3-methoxyphenyl)ethanamine

1.2 Other means of identification

Product number -
Other names (R)-2,2,2-trifluoro-1-(3-methoxyphenyl)ethylamine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1213162-90-3 SDS

1213162-90-3Relevant academic research and scientific papers

Enantiodivergent approach to trifluoromethylated amines: A concise route to both enantiomeric analogues of calcimimetic NPS R-568

Fernandez, Inmaculada,Valdivia, Victoria,Alcudia, Ana,Chelouan, Ahmed,Khiar, Noureddine

experimental part, p. 1502 - 1509 (2010/06/15)

Reported herein is a straightforward and enantiodivergent synthesis of both enantiomers of trifluoromethylated analogues of calcimimetic NPS R-569 in a highly estereoselective manner. The synthesis features a diastereoselective synthesis of the N-(isopropylsulfinyl)imine unit by the "DAG methodology" and a diastereoselective addition of Ruppert Prakash's reagent to the imine as the key steps. No protecting groups were necessary, permitting an atom economic synthesis in only six steps. Further addition reactions of the CF3 anion to different N-(isopropylsulfinyl)imines were performed to demonstrate the suitability of the sulfinyl substituent to balance perfectly reactivity and diastereoselectivity.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 1213162-90-3