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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)-

Guanidine, [4-(4-morpholinyl)phenyl]-

NC(=N)Nc1ccc(cc1)N1CCOCC1 Request for Quotation
Chemical Name: Guanidine, [4-(4-morpholinyl)phenyl]-
CAS Number: 247234-41-9
Product Number: AG002P8T(AGN-PC-0O87VL)
Synonyms:
MDL No:
Molecular Formula: C11H16N4O
Molecular Weight: 220.2709

Identification/Properties

Computed Properties
Molecular Weight:
220.276g/mol
XLogP3:
-0.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
220.132g/mol
Monoisotopic Mass:
220.132g/mol
Topological Polar Surface Area:
76.9A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
238
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:
1
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


1-(4-Morpholinophenyl)guanidine, also known as $name$, is a versatile compound widely used in chemical synthesis as a key building block in organic chemistry. Its unique molecular structure enables its application in a variety of chemical reactions, making it a valuable tool for synthesizing diverse compounds.Due to its high reactivity and selectivity, 1-(4-Morpholinophenyl)guanidine is commonly employed in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. It serves as a crucial intermediate in the production of various bioactive molecules, allowing chemists to efficiently access complex structures that are essential for drug discovery and development.In addition to its role in pharmaceutical chemistry, 1-(4-Morpholinophenyl)guanidine is also utilized in materials science for the preparation of advanced polymers, dyes, and functional materials. Its ability to participate in multiple types of reactions, such as nucleophilic substitutions and condensation processes, makes it an indispensable reagent for creating new compounds with tailored properties.Overall, the versatility and utility of 1-(4-Morpholinophenyl)guanidine in chemical synthesis highlight its importance in modern organic chemistry research and industry applications. Whether in academia or in the laboratory, this compound continues to play a critical role in advancing the field of synthetic chemistry and enabling the development of innovative products and materials.