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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-Morpholinecarboxylic acid, 4-(phenylmethyl)-, (3R)-

OC(=O)[C@H]1COCCN1Cc1ccccc1 Request for Quotation
Chemical Name: 3-Morpholinecarboxylic acid, 4-(phenylmethyl)-, (3R)-
CAS Number: 929047-50-7
Product Number: AG003CA2(AGN-PC-0ONH30)
Synonyms:
MDL No: MFCD06799464
Molecular Formula: C12H15NO3
Molecular Weight: 221.2524

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
221.256g/mol
XLogP3:
-1.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
221.105g/mol
Monoisotopic Mass:
221.105g/mol
Topological Polar Surface Area:
49.8A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
238
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (R)-4-Benzyl-3-morpholinecarboxylic Acid is a chiral building block with valuable applications in chemical synthesis. This compound, with its specific molecular structure, is particularly useful in the creation of various pharmaceuticals and bioactive molecules. Its chiral nature allows for the fine-tuning of stereochemistry in organic reactions, making it a versatile tool in asymmetric synthesis. Additionally, (R)-4-Benzyl-3-morpholinecarboxylic Acid can serve as a key intermediate in the preparation of complex organic compounds, contributing to the development of new drugs and materials. Its role in chemical synthesis highlights its importance in the field of organic chemistry and underscores its potential for advancing scientific research and innovation.