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  2. (2R)-2-[(4-chlorophenyl)methyl]-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid

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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)-

(2R)-2-[(4-chlorophenyl)methyl]-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid

O=C(OC(C)(C)C)NCC(C(=O)O)Cc1ccc(cc1)Cl Request for Quotation
Chemical Name: (2R)-2-[(4-chlorophenyl)methyl]-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
CAS Number: 626220-65-3
Product Number: AG00EAPF(AGN-PC-05VD6C)
Synonyms:
MDL No: MFCD08061164
Molecular Formula: C15H20ClNO4
Molecular Weight: 313.7766

Identification/Properties

Computed Properties
Molecular Weight:
313.778g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
313.108g/mol
Monoisotopic Mass:
313.108g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
359
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 compound 3-((tert-Butoxycarbonyl)amino)-2-(4-chlorobenzyl)propanoic acid, also known as $name$, plays a crucial role in various chemical synthesis applications. Its unique structure and properties make it a valuable reagent in the field of organic chemistry.$name$ is frequently utilized as a protecting group in peptide synthesis. By temporarily shielding the amine group with the tert-butoxycarbonyl (Boc) moiety, $name$ facilitates the selective protection of specific amino acids during peptide bond formation. This allows for controlled sequential deprotection and coupling reactions, leading to the successful assembly of complex peptides with high purity and yield.Moreover, $name$ serves as a versatile building block for the synthesis of bioactive molecules and pharmaceutical compounds. The 4-chlorobenzyl group provides a point of attachment for further modifications, enabling the introduction of various functional groups or structural motifs to tailor the properties of the final product. This flexibility makes $name$ a valuable intermediate in the synthesis of drug candidates, agrochemicals, and other fine chemicals.In organic synthesis, $name$ offers chemists a practical tool for the construction of diverse molecular structures with tailored properties. Its strategic incorporation into synthetic pathways enables the efficient assembly of complex molecules and facilitates the exploration of new chemical reactions and methodologies in the field of organic synthesis.