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(2R)-2-AMINO-2-[4-CHLORO-3-(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL is a chiral compound characterized by an asymmetric carbon atom, featuring an amino group, a chloro group, and a trifluoromethyl group attached to its central carbon. This unique molecular structure endows it with potential applications across various fields, including pharmaceuticals, agrochemicals, and materials science. Its optical activity and specific functional groups may contribute to its reactivity and interactions with biological systems or materials, warranting further research and testing to explore its full potential.

1213168-06-9

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1213168-06-9 Usage

Uses

Used in Pharmaceutical Industry:
(2R)-2-AMINO-2-[4-CHLORO-3-(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL is used as a potential pharmaceutical agent for the development of new drugs. Its unique structure may allow it to interact with specific biological targets, such as enzymes or receptors, which could be leveraged for therapeutic effects. The optical activity of (2R)-2-AMINO-2-[4-CHLORO-3-(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL may also play a role in its efficacy and selectivity, as stereochemistry often influences the pharmacological properties of drugs.
Used in Agrochemical Industry:
In the agrochemical sector, (2R)-2-AMINO-2-[4-CHLORO-3-(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL may be utilized as a precursor or active ingredient in the development of new pesticides or herbicides. Its specific functional groups could enable it to target and control pests or weeds effectively, while its chirality might offer advantages in terms of selectivity and reduced environmental impact.
Used in Materials Science:
(2R)-2-AMINO-2-[4-CHLORO-3-(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL could be employed in materials science for the synthesis of novel materials with unique properties. Its ability to form covalent or non-covalent interactions with other molecules may contribute to the development of advanced materials with applications in areas such as nanotechnology, polymer science, or surface coatings.
Further research and testing are essential to fully understand the potential uses and effects of (2R)-2-AMINO-2-[4-CHLORO-3-(TRIFLUOROMETHYL)PHENYL]ETHAN-1-OL, as its unique structure and properties may offer significant advantages in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1213168-06-9 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 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1213168-06:
(9*1)+(8*2)+(7*1)+(6*3)+(5*1)+(4*6)+(3*8)+(2*0)+(1*6)=109
109 % 10 = 9
So 1213168-06-9 is a valid CAS Registry Number.

1213168-06-9Upstream product

1213168-06-9Downstream Products

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