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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-(chloromethyl)-4-(phenylmethyl)-, (2R)-

ClC[C@@H]1OCCN(C1)Cc1ccccc1 Request for Quotation
Chemical Name: Morpholine, 2-(chloromethyl)-4-(phenylmethyl)-, (2R)-
CAS Number: 186293-54-9
Product Number: AG007SCJ(AGN-PC-0O5IAI)
Synonyms:
MDL No:
Molecular Formula: C12H16ClNO
Molecular Weight: 225.7145

Identification/Properties

Computed Properties
Molecular Weight:
225.716g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
225.092g/mol
Monoisotopic Mass:
225.092g/mol
Topological Polar Surface Area:
12.5A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
183
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


(2R)-2-(Chloromethyl)-4-(phenylmethyl)morpholine is a versatile compound that finds widespread application in chemical synthesis. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique molecular structure offers opportunities for diverse functionalization and reactivity in organic reactions. In particular, it is commonly used in the synthesis of heterocyclic compounds and complex organic molecules due to its chiral center and selective reactivity. Its presence can impart specific stereochemical characteristics to the final products, making it a valuable tool in the hands of synthetic chemists.