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  2. 1-(2-amino-5-chlorophenyl)-2,2,2-trifluoroethanone;hydrate;hydrochloride

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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)-

1-(2-amino-5-chlorophenyl)-2,2,2-trifluoroethanone;hydrate;hydrochloride

O=C(C(F)(F)F)c1cc(Cl)ccc1N.O.Cl Request for Quotation
Chemical Name: 1-(2-amino-5-chlorophenyl)-2,2,2-trifluoroethanone;hydrate;hydrochloride
CAS Number: 1184936-21-7
Product Number: AG003L2B(AGN-PC-0723YJ)
Synonyms:
MDL No: MFCD09841379
Molecular Formula: C8H8Cl2F3NO2
Molecular Weight: 278.0558

Identification/Properties

Properties
MP:
156-158°C
BP:
282.3 °C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
278.052g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
276.988g/mol
Monoisotopic Mass:
276.988g/mol
Topological Polar Surface Area:
44.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
231
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:
3
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Chloro-2-(trifluoroacetyl)aniline Hydrochloride Hydrate finds significant application in chemical synthesis as a versatile building block. With its unique structure and properties, this compound serves as a valuable intermediate in the synthesis of various complex organic compounds. Its trifluoroacetyl group allows for selective and efficient functionalization reactions, enabling the introduction of specific functional groups at desired positions in target molecules. This compound plays a crucial role in the preparation of pharmaceuticals, agrochemicals, and other specialty chemicals where precise control over chemical transformations is essential for the desired product outcome. Its hydrochloride hydrate form ensures stability and ease of handling in a laboratory setting, making it a preferred choice for chemists and researchers involved in synthetic organic chemistry.