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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)-

1H-Benzotriazole, 1-(trifluoroacetyl)-

O=C(C(F)(F)F)n1nnc2c1cccc2 Request for Quotation
Chemical Name: 1H-Benzotriazole, 1-(trifluoroacetyl)-
CAS Number: 183266-61-7
Product Number: AG00ALAO(AGN-PC-0KT19R)
Synonyms:
MDL No:
Molecular Formula: C8H4F3N3O
Molecular Weight: 215.1320696

Identification/Properties

Computed Properties
Molecular Weight:
215.135g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
0
Exact Mass:
215.031g/mol
Monoisotopic Mass:
215.031g/mol
Topological Polar Surface Area:
47.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
268
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:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319
Precautionary Statements:
P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(1H-Benzo[d][1,2,3]triazol-1-yl)-2,2,2-trifluoroethanone is a versatile compound that finds wide application in chemical synthesis. It serves as a valuable building block in the creation of various functional molecules due to its unique structural characteristics. This compound is particularly essential in the development of pharmaceuticals, agrochemicals, and materials science. Its trifluoroethyl group imparts distinct properties that can be exploited in the design of novel compounds with desirable biological or physical attributes. In organic synthesis, the presence of the 1H-benzo[d][1,2,3]triazol-1-yl moiety enables the selective modification of molecules, facilitating the formation of complex structures with enhanced reactivity profiles. Moreover, the trifluoroethanone functionality enhances the chemical stability and lipophilicity of the resulting products, making them suitable for a wide range of applications. This compound's role in chemical synthesis is crucial for the development of innovative materials and bioactive compounds with potential applications across various industries.