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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-Morpholinecarboxylic acid, 2-(aminomethyl)-, 1,1-dimethylethyl ester

NCC1OCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 4-Morpholinecarboxylic acid, 2-(aminomethyl)-, 1,1-dimethylethyl ester
CAS Number: 140645-53-0
Product Number: AG001CNB(AGN-PC-023GNX)
Synonyms:
MDL No: MFCD06410633
Molecular Formula: C10H20N2O3
Molecular Weight: 216.2774

Identification/Properties

Properties
BP:
310.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
216.281g/mol
XLogP3:
-0.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
216.147g/mol
Monoisotopic Mass:
216.147g/mol
Topological Polar Surface Area:
64.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
225
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

GHS Pictogram:
Signal Word:
Danger
UN#:
2810
Hazard Statements:
H301
Precautionary Statements:
P301+P310
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 4-Morpholinecarboxylic acid, 2-(aminomethyl)-, 1,1-dimethylethyl ester is a versatile compound widely used in chemical synthesis. It serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. With its unique structure and reactivity, this compound plays a vital role in the development of new organic molecules with diverse applications.One of the primary applications of 4-Morpholinecarboxylic acid, 2-(aminomethyl)-, 1,1-dimethylethyl ester is in the synthesis of bioactive compounds such as antiviral and antibacterial agents. Its functional groups can be selectively modified to introduce specific properties that enhance the biological activity of the final product. Additionally, this compound is employed in the preparation of advanced materials, including polymers, resins, and dyes, where its reactivity and compatibility with other chemicals are crucial for achieving the desired characteristics.Furthermore, in the field of medicinal chemistry, 4-Morpholinecarboxylic acid, 2-(aminomethyl)-, 1,1-dimethylethyl ester is utilized for the synthesis of prodrugs, which are inactive compounds that undergo chemical transformations in the body to release the active pharmaceutical ingredient. This strategy enables targeted drug delivery, improved pharmacokinetics, and reduced side effects, making it an important tool in the development of pharmaceutical formulations.Overall, the versatility and reactivity of 4-Morpholinecarboxylic acid, 2-(aminomethyl)-, 1,1-dimethylethyl ester make it an indispensable component in modern chemical synthesis, enabling the creation of novel compounds with valuable applications in various industries.