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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)-

[2-fluoro-4-(trifluoromethyl)phenyl]hydrazine;hydrochloride

NNc1ccc(cc1F)C(F)(F)F.Cl Request for Quotation
Chemical Name: [2-fluoro-4-(trifluoromethyl)phenyl]hydrazine;hydrochloride
CAS Number: 1030313-53-1
Product Number: AG003CR4(AGN-PC-0786FQ)
Synonyms:
MDL No:
Molecular Formula: C7H7ClF4N2
Molecular Weight: 230.5905

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
230.591g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
230.023g/mol
Monoisotopic Mass:
230.023g/mol
Topological Polar Surface Area:
38A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
170
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (2-Fluoro-4-(trifluoromethyl)phenyl)hydrazine hydrochloride is a versatile compound widely utilized in chemical synthesis. Its unique molecular structure makes it an ideal reagent for various reactions, particularly in the field of organic chemistry.One key application of (2-Fluoro-4-(trifluoromethyl)phenyl)hydrazine hydrochloride is as a building block for the synthesis of various heterocyclic compounds. Its ability to undergo diverse chemical transformations, such as nucleophilic substitution and oxidative coupling reactions, allows for the efficient formation of complex structures with desired functionalities.Furthermore, (2-Fluoro-4-(trifluoromethyl)phenyl)hydrazine hydrochloride is often employed in the preparation of pharmaceutical intermediates and agrochemicals due to its role in introducing specific functional groups or pharmacophores into target molecules. Its incorporation into the synthesis of bioactive compounds has proven valuable in the development of new drugs and chemical entities with potential therapeutic applications.Overall, the (2-Fluoro-4-(trifluoromethyl)phenyl)hydrazine hydrochloride is a valuable tool in the hands of synthetic chemists, enabling the efficient construction of diverse molecular architectures for various scientific and industrial purposes.