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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)-

tert-butyl (2R)-2-(2-hydroxyethyl)morpholine-4-carboxylate

OCCC1OCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl (2R)-2-(2-hydroxyethyl)morpholine-4-carboxylate
CAS Number: 913642-78-1
Product Number: AG006BO3(AGN-PC-07246P)
Synonyms:
MDL No:
Molecular Formula: C11H21NO4
Molecular Weight: 231.2887

Identification/Properties

Properties
Storage:
2-8℃;Keep in dry area;
Computed Properties
Molecular Weight:
231.292g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
231.147g/mol
Monoisotopic Mass:
231.147g/mol
Topological Polar Surface Area:
59A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
237
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl 2-(2-hydroxyethyl)morpholine-4-carboxylate is a versatile compound used in various chemical synthesis applications. It serves as a valuable building block for the synthesis of complex organic molecules due to its unique structural characteristics and functional groups. This compound can be employed as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its ability to undergo various chemical reactions, such as esterification, amidation, and nucleophilic substitution, makes it a valuable tool for chemists seeking to create novel compounds with specific properties and functionalities. Additionally, the tert-Butyl 2-(2-hydroxyethyl)morpholine-4-carboxylate can be utilized in the development of new drug candidates, specialty chemicals, and polymers, showcasing its importance in the field of chemical synthesis.