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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)-

Benzenecarboximidamide, 3-fluoro-, monohydrochloride

Fc1cccc(c1)C(=N)N.Cl Request for Quotation
Chemical Name: Benzenecarboximidamide, 3-fluoro-, monohydrochloride
CAS Number: 75207-72-6
Product Number: AG00ICM9(AGN-PC-0U6T80)
Synonyms:
MDL No:
Molecular Formula: C7H8ClFN2
Molecular Weight: 174.6032

Identification/Properties

Computed Properties
Molecular Weight:
174.603g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
174.036g/mol
Monoisotopic Mass:
174.036g/mol
Topological Polar Surface Area:
49.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
136
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

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Chemical Structure


3-Fluorobenzimidamide hydrochloride, a versatile compound widely employed in chemical synthesis, is utilized as a key building block in the development of various pharmaceutical and agrochemical products. With its unique molecular structure and reactive properties, this compound serves as a crucial intermediate in the synthesis of complex organic compounds, enabling the creation of novel substances with enhanced biological activities.In chemical synthesis, 3-Fluorobenzimidamide hydrochloride plays a crucial role as a nucleophilic reagent, facilitating the formation of carbon-carbon and carbon-heteroatom bonds through a range of coupling reactions. This compound is particularly valued for its ability to introduce the fluorine atom into target molecules, enabling the modification of their physicochemical properties and enhancing their bioactivity.Furthermore, 3-Fluorobenzimidamide hydrochloride is utilized in the preparation of diverse heterocyclic systems, offering a pathway to structurally diverse compounds with potential applications in medicinal chemistry and material science. Its versatility and synthetic utility make it an indispensable tool for chemists engaged in the design and synthesis of new molecules with desired properties and functions.