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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)-

2-Morpholinemethanamine

NCC1CNCCO1 Request for Quotation
Chemical Name: 2-Morpholinemethanamine
CAS Number: 116143-27-2
Product Number: AG000BR3(AGN-PC-0K4VX5)
Synonyms:
MDL No: MFCD03990581
Molecular Formula: C5H12N2O
Molecular Weight: 116.1616

Identification/Properties

Properties
BP:
202.5°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
116.164g/mol
XLogP3:
-1.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
116.095g/mol
Monoisotopic Mass:
116.095g/mol
Topological Polar Surface Area:
47.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
67.4
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Aminomethyl)morpholine is a versatile compound that finds wide application in chemical synthesis for its unique properties and reactivity. With its amine and morpholine functional groups, this compound plays a crucial role as a building block in the creation of various organic molecules. The amine group in 2-(Aminomethyl)morpholine allows for facile derivatization and functionalization, enabling chemists to introduce a wide range of substituents and modifications. Additionally, the morpholine ring confers stability and steric hindrance, making it an ideal scaffold for diverse molecular constructions. In chemical synthesis, 2-(Aminomethyl)morpholine can serve as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it a valuable tool for synthesizing complex organic molecules with precision and efficiency.