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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)-

3,5-dichlorobenzenecarboximidamide;hydrochloride

NC(=N)c1cc(Cl)cc(c1)Cl.Cl Request for Quotation
Chemical Name: 3,5-dichlorobenzenecarboximidamide;hydrochloride
CAS Number: 22978-61-6
Product Number: AG00BCPA(AGN-PC-0KKCK6)
Synonyms:
MDL No:
Molecular Formula: C7H7Cl3N2
Molecular Weight: 225.5029

Identification/Properties

Computed Properties
Molecular Weight:
225.497g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
223.967g/mol
Monoisotopic Mass:
223.967g/mol
Topological Polar Surface Area:
49.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
151
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3,5-Dichlorobenzimidamide hydrochloride is a versatile compound commonly employed in chemical synthesis for its pivotal role as a building block in various reactions. One notable application of this compound is its utilization as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its unique chemical structure enables it to participate in a range of reactions, facilitating the formation of complex molecular structures. Furthermore, 3,5-Dichlorobenzimidamide hydrochloride exhibits excellent stability and reactivity, making it a valuable component in the creation of new compounds with diverse functionalities. In the realm of chemical synthesis, this compound serves as a fundamental tool for the design and production of advanced materials with enhanced properties and applications.