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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)-

L-Alanine, N-[(phenylmethoxy)carbonyl]-L-alanyl-

C[C@@H](C(=O)N[C@H](C(=O)O)C)NC(=O)OCc1ccccc1 Request for Quotation
Chemical Name: L-Alanine, N-[(phenylmethoxy)carbonyl]-L-alanyl-
CAS Number: 16012-70-7
Product Number: AG001ROF(AGN-PC-0O4KOB)
Synonyms:
MDL No:
Molecular Formula: C14H18N2O5
Molecular Weight: 294.3031

Identification/Properties

Computed Properties
Molecular Weight:
294.307g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
7
Exact Mass:
294.122g/mol
Monoisotopic Mass:
294.122g/mol
Topological Polar Surface Area:
105A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
380
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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


Z-Ala-Ala-OH is a dipeptide derivative commonly used in chemical synthesis as a building block for the creation of peptides and pharmaceutical compounds. This compound, consisting of the amino acids alanine linked together, serves as a key intermediate in peptide synthesis due to its stability and versatile reactivity.In chemical synthesis, Z-Ala-Ala-OH is utilized as a protected peptide, with the "Z" group acting as a protective moiety for the amino group of the alanine residues. This protective group prevents unwanted side reactions during peptide bond formation, allowing for precise and controlled assembly of longer peptide chains.Furthermore, Z-Ala-Ala-OH can also be functionalized and modified at various sites to introduce specific chemical functionalities or structural motifs, enabling the design and development of novel peptide-based drugs or biologically active molecules with tailored properties.Overall, the application of Z-Ala-Ala-OH in chemical synthesis provides chemists with a valuable tool for the efficient and customizable construction of peptides and organic compounds in pharmaceutical research and development.