35661-39-3 | Fmoc-Ala-OH

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$8.00	$5.00
10g	98%	in stock	$9.00	$6.00
25g	98%	in stock	$10.00	$7.00
100g	98%	in stock	$28.00	$19.00

Description

• Catalog Number: AI48782
• Chemical Name: Fmoc-Ala-OH
• CAS Number: 35661-39-3
• Molecular Formula: C18H17NO4
• Molecular Weight: 311.33187999999996
• MDL Number: MFCD00150487
• SMILES: O=C(N[C@H](C(=O)O)C)OCC1c2ccccc2-c2c1cccc2

Computed Properties

• Complexity: 430
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 23
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 5
• XLogP3: 3.1

Upstream Synthesis Route

Fmoc-L-Alanine is a key component used in chemical synthesis, particularly in the field of peptide synthesis. This compound serves as a versatile building block for creating peptides, which are important molecules in drug development, biological research, and various other applications. By selectively protecting the amino group with the Fmoc (fluorenylmethyloxycarbonyl) group, Fmoc-L-Alanine enables precise control over the sequential assembly of amino acids in the peptide chain. Through solid-phase peptide synthesis methodologies, Fmoc-L-Alanine can be incorporated into peptides with high purity and yield, making it essential for the creation of custom peptides with specific sequences and properties. Additionally, the Fmoc-L-Alanine derivative offers compatibility with common coupling reagents and deprotection conditions, streamlining the synthesis process and enhancing efficiency for researchers and chemists in both academic and industrial settings.

Literature

• Structural determinants of integrin binding to the talin rod.

  The Journal of biological chemistry 20090327

• Separation and measurement of plant alkaloid enantiomers by RP-HPLC analysis of their Fmoc-Alanine analogs.

  Phytochemical analysis : PCA 20080101

• Chiral analysis of biogenic DL-amino acids derivatized by urethane - protected alpha-amino acid N-carboxyanhydride using capillary zone electrophoresis and micellar electrokinetic chromatography.

  Electrophoresis 20020801