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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)-

4-nitrobenzenecarboximidamide;hydrochloride

NC(=N)c1ccc(cc1)[N+](=O)[O-].Cl Request for Quotation
Chemical Name: 4-nitrobenzenecarboximidamide;hydrochloride
CAS Number: 15723-90-7
Product Number: AG001PAZ(AGN-PC-0JPRHH)
Synonyms:
MDL No: MFCD00278833
Molecular Formula: C7H8ClN3O2
Molecular Weight: 201.6103

Identification/Properties

Properties
MP:
286-288°C
BP:
310.6°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Solid
Computed Properties
Molecular Weight:
201.61g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
201.031g/mol
Monoisotopic Mass:
201.031g/mol
Topological Polar Surface Area:
95.7A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
191
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


4-Nitrobenzamidine Hydrochloride is a versatile compound commonly used in chemical synthesis as a key reagent and building block. With its strong nucleophilic properties, this compound is highly valued in the field of organic chemistry for the efficient and selective formation of various functionalized compounds. Its ability to react with a wide range of electrophiles makes it an essential tool for the creation of diverse molecular structures and complex organic molecules. Additionally, 4-Nitrobenzamidine Hydrochloride is frequently employed in medicinal chemistry research for the synthesis of potential pharmaceutical agents due to its unique reactivity and functional group compatibility. By incorporating this compound into synthetic routes, chemists can access new pathways for the development of novel drug candidates and bioactive molecules. In conclusion, 4-Nitrobenzamidine Hydrochloride plays a critical role in advancing chemical synthesis and expanding the possibilities for molecular design and discovery in various scientific fields.