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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)-

2,4-Morpholinedicarboxylic acid, 4-(1,1-dimethylethyl) ester

[O-]C(=O)C1OCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 2,4-Morpholinedicarboxylic acid, 4-(1,1-dimethylethyl) ester
CAS Number: 189321-66-2
Product Number: AG002I9J(AGN-PC-05WL9O)
Synonyms:
MDL No:
Molecular Formula: C10H16NO5-
Molecular Weight: 230.2377

Identification/Properties

Properties
MP:
>139ºC (dec.)
BP:
369.473 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
231.248g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
231.111g/mol
Monoisotopic Mass:
231.111g/mol
Topological Polar Surface Area:
76.1A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
283
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:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Boc-2-morpholinecarboxylic acid is a versatile compound commonly used in chemical synthesis as a protecting group for amines. This compound is a key building block in peptide synthesis, where it is employed to temporarily block the amino group of amino acids. By attaching the Boc protecting group to the amine, it prevents unwanted reactions during subsequent steps of the synthesis process. This protection can be easily removed under mild acidic conditions, revealing the free amine for further chemical manipulations.Moreover, 4-Boc-2-morpholinecarboxylic acid is also utilized in medicinal chemistry to modify and design new drug molecules. Its ability to selectively protect primary amines makes it a valuable tool in the development of pharmaceutical compounds. The versatility and efficiency of this compound make it a crucial component in the production of various organic molecules with specific functions and properties.