Boc-L-Alanine Methyl Ester|28875-17-4,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-

Boc-L-Alanine Methyl Ester

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Chemical Name:	Boc-L-Alanine Methyl Ester
CAS Number:	28875-17-4
Product Number:	AG002WWP(AGN-PC-0WACNT)
Synonyms:
MDL No:
Molecular Formula:	C9H17NO4
Molecular Weight:	203.2356

Identification/Properties
Safety Information
NMR Spectrum
Other Analytical Data
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Identification/Properties

Properties

MP:

32-35 °C(lit.)

BP:

277.8°C at 760 mmHg

Storage:

Keep in dry area;Room Temperature;

Form:

Solid

Refractive Index:

1.4315 (estimate)

Computed Properties

Molecular Weight:

203.238g/mol

XLogP3:

0.8

Hydrogen Bond Donor Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

Exact Mass:

203.116g/mol

Monoisotopic Mass:

203.116g/mol

Topological Polar Surface Area:

64.6A^2

Heavy Atom Count:

Formal Charge:

Complexity:

219

Isotope Atom Count:

Defined Atom Stereocenter Count:

Undefined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Undefined Bond Stereocenter Count:

Covalently-Bonded Unit Count:

Compound Is Canonicalized:

Yes

Safety Information

GHS Pictogram:

Signal Word:

Warning

UN#:

Hazard Statements:

H315-H319-H335

Precautionary Statements:

P261-P305+P351+P338

Class:

Packing Group:

NMR Spectrum

Other Analytical Data

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Chemical Structure

Boc-Ala-OMe, N-tert-butoxycarbonyl-L-alanine methyl ester, is a widely used building block in organic synthesis with versatile applications in chemical transformations. This compound serves as a crucial derivative of alanine, an amino acid essential for the formation of peptides and proteins. In chemical synthesis, Boc-Ala-OMe plays a significant role as a protected amino acid, providing a means to control and manipulate the reactivity of the amino group.One of the key applications of Boc-Ala-OMe is its use as a substrate for peptide synthesis. By selectively deprotecting the Boc group under controlled conditions, the amino acid can be incorporated into a growing peptide chain through peptide coupling reactions. This strategy allows for the specific incorporation of alanine residues at desired positions within a peptide sequence, enabling the construction of complex peptide structures with precise control over sequence and functionality.Furthermore, Boc-Ala-OMe can also serve as a valuable intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals. Its compatibility with a wide range of synthetic methodologies makes it a versatile tool for the preparation of diverse molecular architectures. Additionally, the Boc protecting group provides stability to the amino acid functionality, preventing unwanted side reactions during synthetic transformations.Overall, the strategic use of Boc-Ala-OMe in chemical synthesis enables chemists to efficiently access and modify alanine-containing molecules, making it an indispensable building block for the construction of complex organic compounds.