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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)-

Benzoic acid, 2-(trifluoromethyl)-, hydrazide

NNC(=O)c1ccccc1C(F)(F)F Request for Quotation
Chemical Name: Benzoic acid, 2-(trifluoromethyl)-, hydrazide
CAS Number: 344-95-6
Product Number: AG007FEF(AGN-PC-0KKY7U)
Synonyms:
MDL No:
Molecular Formula: C8H7F3N2O
Molecular Weight: 204.1492

Identification/Properties

Computed Properties
Molecular Weight:
204.152g/mol
XLogP3:
0.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
1
Exact Mass:
204.051g/mol
Monoisotopic Mass:
204.051g/mol
Topological Polar Surface Area:
55.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
217
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Trifluoromethyl)benzohydrazide is a versatile compound frequently used in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials due to its ability to introduce the trifluoromethyl functional group into organic molecules. This modification often leads to enhanced biological activities and improved physicochemical properties of the final product. Additionally, 2-(Trifluoromethyl)benzohydrazide can participate in diverse chemical reactions such as nucleophilic additions, radical reactions, and transition metal-catalyzed transformations, making it a valuable tool for synthetic chemists seeking to craft complex molecular structures. Its versatility and reactivity in chemical synthesis make it a valuable asset in the development of novel compounds with promising applications across various fields of science and industry.