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CS-W001157 4
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(S)-3-(1-((tert-Butoxycarbonyl)amino)ethyl)benzoic acid

  • CAS No. 1187930-10-4

  • Cat. No. CS-0158264
  • Purity≥95%
  • MDL No.MFCD12913673

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

(S)-3-(1-((tert-Butoxycarbonyl)amino)ethyl)benzoic acid|CS-0158264

Structure of 1187930-10-4

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General Information

  • CAS No. 1187930-10-4
  • Cat. No. CS-0158264
  • Purity ≥95%
  • MDL No. MFCD12913673
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₄H₁₉NO₄
  • Molecular Weight 265.30
  • Synonym(s) (S)-3-(1-tert-Butoxycarbonylamino-ethyl)-benzoic acid
  • SMILES C[C@@H](C1=CC(=CC=C1)C(=O)O)NC(=O)OC(C)(C)C

Description

(S)-3-(1-((tert-Butoxycarbonyl)amino)ethyl)benzoic acid is a chiral building block featuring a protected amino group and a carboxylic acid handle, enabling straightforward incorporation into peptide and bioactive molecule synthesis under standard conditions.

Application

(S)-3-(1-((tert-Butoxycarbonyl)amino)ethyl)benzoic acid serves as a versatile chiral building block for medicinal chemistry and peptide synthesis. The protected amine and carboxylic acid functionalities enable sequential coupling reactions, while the (S)-stereocenter provides defined stereochemical control. Bench-stable and readily purified by standard chromatographic methods, it functions effectively in solution-phase synthesis of bioactive heterocycles and peptidomimetics.

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-H312-H332
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501

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Computational Chemistry Data

  • TPSA   75.63
  • LogP   2.9705
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   3

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