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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)-

5-bromopyridine-2-carboximidamide;hydrochloride

Brc1ccc(nc1)C(=N)N.Cl Request for Quotation
Chemical Name: 5-bromopyridine-2-carboximidamide;hydrochloride
CAS Number: 1179361-93-3
Product Number: AG008ZYT(AGN-PC-09TPC8)
Synonyms:
MDL No:
Molecular Formula: C6H7BrClN3
Molecular Weight: 236.4969

Identification/Properties

Computed Properties
Molecular Weight:
236.497g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
234.951g/mol
Monoisotopic Mass:
234.951g/mol
Topological Polar Surface Area:
62.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
137
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


5-Bromopicolinimidamide hydrochloride is a versatile chemical reagent commonly employed in chemical synthesis procedures for its unique properties and practical applications. One key use of this compound is as a valuable building block for the synthesis of various heterocyclic molecules and pharmaceutical intermediates. It serves as a crucial reagent in the construction of complex organic compounds due to its ability to undergo specific reactions that facilitate the formation of new chemical bonds. Furthermore, 5-Bromopicolinimidamide hydrochloride plays a vital role in the development of novel drug candidates and agrochemicals, showcasing its significance in the field of medicinal and agricultural chemistry. Its compatibility with a wide range of reaction conditions and functional groups makes it a highly sought-after reagent for the efficient and controlled synthesis of target molecules with diverse applications in the chemical industry.