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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)-

Morpholine,2-(methoxymethyl)-, (2R)-

COC[C@H]1CNCCO1 Request for Quotation
Chemical Name: Morpholine,2-(methoxymethyl)-, (2R)-
CAS Number: 157791-21-4
Product Number: AG001PP0(AGN-PC-0Q7CXC)
Synonyms:
MDL No:
Molecular Formula: C6H13NO2
Molecular Weight: 131.1729

Identification/Properties

Computed Properties
Molecular Weight:
131.175g/mol
XLogP3:
-0.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
131.095g/mol
Monoisotopic Mass:
131.095g/mol
Topological Polar Surface Area:
30.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
77.5
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H319
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(2R)-2-(Methoxymethyl)morpholine is a valuable chemical compound widely used in organic synthesis due to its versatile reactivity and unique structural properties. This compound serves as a valuable building block in the production of various pharmaceuticals, agrochemicals, and functional materials. Its cyclohexane ring structure and methoxymethyl functional group make it an ideal precursor for the synthesis of complex molecules with biological activities.In chemical synthesis, (2R)-2-(Methoxymethyl)morpholine can be utilized as a masked amine functionality, where the morpholine ring acts as a protecting group for the amino group. By selectively deprotecting the morpholine under specific reaction conditions, the free amine can then participate in subsequent transformations, such as amidation, alkylation, or cyclization reactions. This strategy allows for the controlled manipulation of amine groups in a molecule, enabling the synthesis of structurally diverse compounds with desired properties.Additionally, the methoxymethyl group in (2R)-2-(Methoxymethyl)morpholine can serve as a versatile handle for further derivatization through various chemical reactions. Functionalization of the methoxymethyl group can lead to the introduction of different substituents or linkers, enhancing the diversity and complexity of the synthesized molecules. This flexibility makes (2R)-2-(Methoxymethyl)morpholine a valuable tool in the synthesis of pharmaceutical intermediates and bioactive compounds with tailored properties.Overall, the strategic incorporation of (2R)-2-(Methoxymethyl)morpholine in chemical synthesis offers synthetic chemists a powerful tool for the construction of complex molecules with precise control over functional group manipulations, ultimately facilitating the discovery and development of novel compounds with potential therapeutic applications.