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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)-

3,4-Morpholinedicarboxylic acid, 4-(1,1-dimethylethyl) ester

OC(=O)C1COCCN1C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 3,4-Morpholinedicarboxylic acid, 4-(1,1-dimethylethyl) ester
CAS Number: 212650-43-6
Product Number: AG003KUA(AGN-PC-09SH15)
Synonyms:
MDL No:
Molecular Formula: C10H17NO5
Molecular Weight: 231.2457

Identification/Properties

Properties
MP:
38-40°C
BP:
369.5 °C at 760 mmHg
Storage:
Keep in dry area;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:
H319-H412
Precautionary Statements:
P273-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Boc-3-Morpholinecarboxylic acid is a versatile compound widely used in chemical synthesis as a key building block in various reactions. Its Boc (tert-butoxycarbonyl) protecting group renders it a valuable tool for organic chemists seeking to control the reactivity of amine functionalities in their synthetic pathways. This compound is particularly valuable in peptide synthesis, where it can be incorporated as a protected amino acid to facilitate the selective formation of peptide bonds. Additionally, 4-Boc-3-Morpholinecarboxylic acid can serve as a precursor for the preparation of complex heterocyclic compounds and pharmaceutical intermediates due to its unique structure and reactivity. Its compatibility with a wide range of coupling reagents and reaction conditions further enhances its utility in the synthesis of diverse organic molecules.