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CS-W001157 4
Total: USD 88.00

Fmoc-Ala-OMe

  • CAS No. 146346-88-5

  • Cat. No. CS-0041006
  • Purity≥97%
  • MDL No.MFCD20264827

*For research and further manufacturing use only, not for direct human use.

Fmoc-Ala-OMe|CS-0041006

Structure of 146346-88-5

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General Information

  • CAS No. 146346-88-5
  • Cat. No. CS-0041006
  • Purity ≥97%
  • MDL No. MFCD20264827
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₉H₁₉NO₄
  • Molecular Weight None
  • Synonym(s) Nα-Fmoc-Ala-OMe
  • SMILES C[C@@H](C(OC)=O)NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O

Description

Fmoc-Ala-OMe is a protected alanine derivative featuring a fluorenylmethoxycarbonyl (Fmoc) group at the N-terminus and methyl ester functionality at the C-terminus. This combination enables efficient incorporation into solid-phase peptide synthesis workflows, offering stability during coupling steps and ease of deprotection under mild basic conditions. The molecule’s bench-stable nature supports reliable handling in routine laboratory settings.

Application

Fmoc-Ala-OMe serves as a robust building block for peptide synthesis, enabling efficient N-terminal protection and orthogonal deprotection in solid-phase and solution-phase workflows. The fluorenylmethoxycarbonyl (Fmoc) group ensures stable protection under basic conditions, while the methyl ester facilitates straightforward conversion to carboxylic acid derivatives. Its bench-stable nature and compatibility with standard coupling reagents make it ideal for iterative peptide assembly and fragment condensation.

Safety Information

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GHS Pictogram : N/A
GHS No : N/A
Signal Word : N/A
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : N/A
Precautionary Statements : N/A

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Computational Chemistry Data

  • TPSA   64.63
  • LogP   3.0866
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   4

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