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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-Morpholinecarboximidamide, monohydrochloride

NC(=N)N1CCOCC1.Cl Request for Quotation
Chemical Name: 4-Morpholinecarboximidamide, monohydrochloride
CAS Number: 5638-78-8
Product Number: AG0039K4(AGN-PC-0SLJ8P)
Synonyms:
MDL No:
Molecular Formula: C5H12ClN3O
Molecular Weight: 165.6213

Identification/Properties

Computed Properties
Molecular Weight:
165.621g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
165.067g/mol
Monoisotopic Mass:
165.067g/mol
Topological Polar Surface Area:
62.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
109
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-Morpholinecarboximidamide monohydrochloride is a versatile compound commonly used in chemical synthesis as a key building block in various organic reactions. With its unique chemical structure, this compound serves as a precursor for the synthesis of diverse pharmaceutical intermediates, agrochemicals, and specialty chemicals. Its reactivity and functional group compatibility make it an essential component in the development of complex organic molecules. In the realm of chemical synthesis, 4-Morpholinecarboximidamide monohydrochloride plays a crucial role in forming bonds, introducing specific functionalities, and influencing the overall stereochemistry of the target molecules. Its application extends to the production of fine chemicals, drug discovery, and material science research, highlighting its significance in advancing modern organic synthesis methodologies.