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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methylpentanoic acid

  • CAS No. 266318-79-0

  • Cat. No. CS-0060833
  • Purity≥97%
  • MDL No.None
  • HazMat Fee +

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    Each bottle is packed as an Excepted Quantity, with a maximum of 1g for items in class 6.1 packing group I or II, and up to 25g for all other hazardous materials.

    If shipping is charged to your FedEx account, the HazMat fee will be billed directly by the courier. Otherwise, the fee will be included on your invoice. To help you avoid the HazMat fee, we can package a 5g order of a class 6.1 packing group I or II material as five separate 1g units, and a 100g order of any other dangerous good as four 25g units. This packaging adjustment will be made unless you instruct otherwise on your purchase order. Below, you will find the fee schedule from FedEx for handling hazardous materials.

    Type
    HazMat Fee
    Excepted Quantity $0.00
    FedEx Limited Quantities Ground $0.00
    Hazmat Ground shipping $50.00+
    Inaccessible (Haz class 6.1 or 9), Domestic $68.00+
    Accessible (Haz class 3, 4, 5 or 8), Domestic $158.00+
    Inaccessible (Haz class 6.1 or 9), International $108.00+
    Accessible (Haz class 3, 4, 5 or 8), International $238.00+

    An item is classified as a dangerous good if our website displays Hazardous Material (HazMat) information for it.

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

(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methylpentanoic acid|CS-0060833

Structure of 266318-79-0

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Description

N-Fmoc-(S)-3-amino-4-methylpentanoic acid features a chiral, side-chain-functionalized amino acid scaffold with a bulky methyl substituent. This configuration enhances steric differentiation in peptide synthesis, while the Fmoc group enables efficient N-terminal protection and orthogonal deprotection. The pendant amine facilitates conjugation or branching in macrocyclic and peptidomimetic architectures.

Application

N-Fmoc-(S)-3-amino-4-methylpentanoic acid serves as a versatile building block for peptide synthesis and medicinal chemistry applications. The Fmoc group enables efficient orthogonal protection during solid-phase peptide coupling, while the (S)-configured amino group and branched aliphatic side chain provide structural diversity for bioactive molecule design. Its bench-stable nature and compatibility with standard deprotection protocols facilitate reliable incorporation into complex scaffolds.

General Information

  • CAS No. 266318-79-0
  • Cat. No. CS-0060833
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₁H₂₃NO₄
  • Molecular Weight 353.41
  • Synonym(s) (S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methylpentanoic acid
  • SMILES CC([C@@H](NC(OCC1C2=CC=CC=C2C3=CC=CC=C31)=O)CC(O)=O)C

Computational Chemistry Data

  • TPSA   75.63
  • LogP   4.0244
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   6

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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