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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-(bromomethyl)-, 1,1-dimethylethyl ester,(2S)-

BrC[C@H]1OCCN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 4-Morpholinecarboxylic acid, 2-(bromomethyl)-, 1,1-dimethylethyl ester,(2S)-
CAS Number: 919286-71-8
Product Number: AG00IGYE(AGN-PC-0VXA2L)
Synonyms:
MDL No:
Molecular Formula: C10H18BrNO3
Molecular Weight: 280.1588

Identification/Properties

Computed Properties
Molecular Weight:
280.162g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
279.047g/mol
Monoisotopic Mass:
279.047g/mol
Topological Polar Surface Area:
38.8A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
227
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
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


The (S)-tert-Butyl 2-(bromomethyl)morpholine-4-carboxylate compound is a versatile building block in chemical synthesis. It can serve as a key intermediate in the preparation of various biologically active molecules and pharmaceutical compounds. Due to its unique structure and reactivity, this compound is commonly employed in the development of new organic reactions and methodologies. Specifically, it can be used in the synthesis of complex heterocyclic compounds and as a chiral auxiliary for asymmetric synthesis. Additionally, (S)-tert-Butyl 2-(bromomethyl)morpholine-4-carboxylate is valuable for the modification of natural products and drug molecules, enabling the creation of novel derivatives with improved pharmacological properties. Its application in chemical synthesis offers a pathway to accessing diverse chemical space and advancing drug discovery efforts.