1. Home
  2. 2-(2,2,2-Trifluoroethoxy)ethanamine hydrochloride

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-(2,2,2-Trifluoroethoxy)ethanamine hydrochloride

NCCOCC(F)(F)F.Cl Request for Quotation
Chemical Name: 2-(2,2,2-Trifluoroethoxy)ethanamine hydrochloride
CAS Number: 1035041-75-8
Product Number: AG00HA35(AGN-PC-0WAKD6)
Synonyms:
MDL No:
Molecular Formula: C4H9ClF3NO
Molecular Weight: 179.5686

Identification/Properties

Computed Properties
Molecular Weight:
179.567g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
179.032g/mol
Monoisotopic Mass:
179.032g/mol
Topological Polar Surface Area:
35.2A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
72.7
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2-(2,2,2-Trifluoroethoxy)ethanamine hydrochloride, commonly referred to as $name$, serves as a versatile reagent in chemical synthesis due to its unique chemical properties. This compound is widely utilized in the pharmaceutical industry as a valuable building block for the synthesis of various drugs and bioactive molecules. The presence of the trifluoroethoxy group enhances the compound's reactivity and stability, making it a valuable tool in organic chemistry.One of the key applications of 2-(2,2,2-Trifluoroethoxy)ethanamine hydrochloride is in the preparation of fluorinated organic compounds. The trifluoroethoxy group can serve as a masked fluorine source in organic reactions, allowing for the introduction of fluorine atoms into target molecules. This fluorination process plays a crucial role in drug development, as fluorinated compounds often exhibit enhanced biological activity and metabolic stability.Additionally, 2-(2,2,2-Trifluoroethoxy)ethanamine hydrochloride can be employed in the synthesis of complex heterocyclic compounds and functionalized amines. By strategically incorporating this reagent into synthetic routes, chemists can access a wide range of structurally diverse compounds with potential pharmacological applications. Overall, the unique properties of $name$ make it a valuable asset in the field of chemical synthesis, enabling the efficient construction of intricate molecular structures for various scientific and industrial purposes.