CAS 71989-16-7

FMOC-L-asparagine

Description:

FMOC-L-asparagine is a derivative of the amino acid asparagine, characterized by the presence of a 9-fluorenylmethoxycarbonyl (FMOC) protective group. This modification enhances its stability and solubility, making it particularly useful in peptide synthesis and other biochemical applications. The FMOC group is known for its ability to be easily removed under mild basic conditions, allowing for selective deprotection during the synthesis of peptides. FMOC-L-asparagine retains the essential properties of asparagine, including its polar side chain, which can participate in hydrogen bonding and contribute to protein structure and function. This compound is typically utilized in research and industrial settings, particularly in the synthesis of peptides where the protection of the amino group is necessary to prevent unwanted reactions. Additionally, FMOC-L-asparagine is soluble in organic solvents and water, facilitating its use in various chemical reactions and formulations. Overall, FMOC-L-asparagine serves as a valuable building block in the field of organic and medicinal chemistry.

Formula: C₁₉H₁₈N₂O₅

InChI: InChI=1S/C19H18N2O5/c20-17(22)9-16(18(23)24)21-19(25)26-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16H,9-10H2,(H2,20,22)(H,21,25)(H,23,24)/t16-/m0/s1

InChI key: InChIKey=YUGBZNJSGOBFOV-INIZCTEOSA-N

SMILES: C(OC(N[C@@H](CC(N)=O)C(O)=O)=O)C1C=2C(C=3C1=CC=CC3)=CC=CC2

Synonyms:

• (2S)-3-Carbamoyl-2-([[(9H-fluoren-9-yl)methoxy]carbonyl]amino)propanoic acid
• (2S)-4-Amino-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxobutanoic acid
• (2S)-4-amino-2-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-4-oxobutanoate
• <span class="text-smallcaps">L</span>-Asparagine, N²-[(9H-fluoren-9-ylmethoxy)carbonyl]-
• FMOC-<span class="text-smallcaps">L</span>-asparagine
• Fmoc-Asn-OH
• Fmoc-L-asparagine
• N-(9-Fluorenylmethoxycarbonyl)asparagine
• N-FMOC-<span class="text-smallcaps">L</span>-asparagine
• N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-asparagine
• N²-(9-Fluorenylmethoxycarbonyl)asparagine
• N²-[(9H-Fluoren-9-ylmethoxy)carbonyl]-<span class="text-smallcaps">L</span>-asparagine
• NSC 334297
• Nalpha-Fmoc-L-Asparagine
• N~2~-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-asparagine
• N~2~-[(9H-fluoren-9-ylmethoxy)carbonyl]asparagine
• N2-(9-Fluorenylmethoxycarbonyl)asparagine

Nα-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-asparagine

CAS: 71989-16-7

Formula: C₁₉H₁₈N₂O₅

Purity: >98.0%(T)

Color and Shape: White to Almost white powder to crystal

Molecular weight: 354.36

Ref: 3B-F0306

Fmoc-Asn-OH

CAS: 71989-16-7

Formula: C₁₉H₁₈N₂O₅

Purity: 97%

Color and Shape: Solid

Molecular weight: 354.3566

Ref: IN-DA003QMT

Fmoc-Asn-OH

CAS: 71989-16-7

Fmoc-Asn-OH

Formula: C₁₉H₁₈N₂O₅

Purity: 98%

Color and Shape: white to off-white powder

Molecular weight: 354.36g/mol

Ref: 54-OR1013333

Fmoc-Asn-OH

CAS: 71989-16-7

Formula: C₁₉H₁₈N₂O₅

Molecular weight: 354.36

Ref: 7W-GM3743

Fmoc-L-Asn-OH

CAS: 71989-16-7

Fmoc-L-Asn-OH is an organic compound that belongs to the group of amides. It reacts with a reactive site in the molecule and is able to form an amide bond. Fmoc-L-Asn-OH has been shown to be effective in the treatment of Alzheimer's disease by inhibiting the formation of beta-amyloid plaques. This compound has also been shown to have a role in cancer prevention, as it can inhibit tumor growth and reduce tumor size. Fmoc-L-Asn-OH can be used as a potential antiinflammatory agent because its mechanism studies have revealed that it inhibits prostaglandin synthesis.

Formula: C₁₉H₁₈N₂O₅

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 354.36 g/mol

Ref: 3D-FF37441

Fmoc-Asn-OH

CAS: 71989-16-7

M03351 - Fmoc-Asn-OH

Formula: C₁₉H₁₈N₂O₅

Purity: 97%

Color and Shape: Solid

Molecular weight: 354.362

Ref: 10-M03351

FMOC-L-Asparagine extrapure, 99%

CAS: 71989-16-7

Formula: C₁₉H₁₈N₂O₅

Purity: min. 99%

Color and Shape: White to Slight yellow, Crystalline powder

Molecular weight: 354.40

Ref: SR-66815