CAS 98045-03-5

N-boc Asp(OH)Ome

Description:

N-Boc Asp(OH)Ome, also known as N-tert-butoxycarbonyl aspartic acid methyl ester, is a derivative of aspartic acid, an amino acid that plays a crucial role in various biological processes. This compound features a tert-butoxycarbonyl (Boc) protecting group, which is commonly used in peptide synthesis to protect the amino group from unwanted reactions. The presence of the hydroxyl (OH) group on the side chain indicates that it is a modified form of aspartic acid, enhancing its reactivity and potential applications in organic synthesis. The methyl ester (Ome) functionality suggests that it can be hydrolyzed to release aspartic acid, making it useful in peptide synthesis and other chemical reactions. N-Boc Asp(OH)Ome is typically a white to off-white solid and is soluble in organic solvents, which facilitates its use in various chemical reactions. Its stability and reactivity make it a valuable intermediate in the synthesis of peptides and other bioactive compounds.

Synonyms:

• Boc-Asp-OMe

1-Methyl N-(tert-Butoxycarbonyl)-L-aspartate

CAS: 98045-03-5

Formula: C₁₀H₁₇NO₆

Purity: >97.0%(T)(HPLC)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 247.25

Ref: 3B-M2970

N-Boc-L-aspartic acid 1-methyl ester, 98%

CAS: 98045-03-5

N-Boc-L-aspartic acid 1-methyl ester is used as an intermediate in the preparation of modified alfa-amino acids and 5-cis-alkylprolines. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the

Formula: C₁₀H₁₇NO₆

Purity: 98%

Molecular weight: 247.25

Ref: 02-H62590

(3S)-3-{[(tert-butoxy)carbonyl]amino}-4-methoxy-4-oxobutanoic acid

CAS: 98045-03-5

Formula: C₁₀H₁₇NO₆

Purity: 97%

Color and Shape: Solid

Molecular weight: 247.2451

Ref: IN-DA00IK0T

Boc-Asp-Ome

CAS: 98045-03-5

Boc-Asp-Ome

Purity: 99%

Molecular weight: 247.25g/mol

Ref: 54-OR1012481

Boc-Asp-OMe

CAS: 98045-03-5

Boc-Asp-OMe is a peptidomimetic that mimics the hydrogen bonding pattern of aspartic acid. It has been shown to have an intramolecular sequence, which can be cyclic or non-cyclic, and an enantioselective conformation. Boc-Asp-OMe is able to form a hydrogen bond with its neighboring amino acid in the peptide chain and is hydrophobic due to its organic chemistry. This molecule also has a phenyl ring with a carbon bond, which can form n-glycosylations. The conformational and stereochemical properties of this molecule are dependent on the environment it is in.

Formula: C₁₀H₁₇NO₆

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 247.25 g/mol

Ref: 3D-FB72153

Boc-Asp-Ome

CAS: 98045-03-5

M06171 - Boc-Asp-Ome

Formula: C₁₀H₁₇NO₆

Purity: 97%

Color and Shape: White powder

Molecular weight: 247.247

Ref: 10-M06171