29834-76-2

Basic information

• Product Name: (S)-2-Amino-4-hexynoic acid
• Synonyms: (S)-2-Amino-4-hexynoic acid;L-Butynylglycine;(S)-2-AMinohex-4-ynoic acid;(2S)-2-Amino-4-hexynoic acid;L-2-Amino-4-hexynoic acid
• CAS NO: 29834-76-2
• Molecular Formula: C₆H₉NO₂
• Molecular Weight: 127.14
• Mol File: 29834-76-2.mol
• Article Data: 1

Chemical Properties

• Melting Point: 238-240℃
• Boiling Point: 264.4±35.0 °C(Predicted)
• Appearance: /
• Density: 1.160±0.06 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 2.06±0.10(Predicted)
• CAS DataBase Reference: (S)-2-Amino-4-hexynoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-Amino-4-hexynoic acid(29834-76-2)
• EPA Substance Registry System: (S)-2-Amino-4-hexynoic acid(29834-76-2)

Safety Data

• Hazardous Substances Data: 29834-76-2(Hazardous Substances Data)

Usage

General Description

(S)-2-Amino-4-hexynoic acid, also known as L-homopropargylglycine, is an organic compound with the molecular formula C6H9NO2. It is an amino acid derivative with a unique structure that contains both an amino group and an alkyne functional group. (S)-2-Amino-4-hexynoic acid has been studied for its potential pharmacological properties, including its ability to inhibit the enzyme γ-aminobutyric acid transaminase and its potential role in regulating neurotransmitter levels in the brain. Additionally, (S)-2-Amino-4-hexynoic acid has been investigated for its potential use in the synthesis of novel pharmaceutical compounds. Overall, this compound has shown promise as a valuable building block in the development of new drugs and as a potential therapeutic agent for various medical applications.

Upstream product

• 100-52-7 benzaldehyde 
• 346707-59-3 (R)-2-tert-butoxycarbonylamino-hex-4-ynoic acid 

Downstream Products

• 346707-61-7 (S)-2-tert-butoxycarbonylamino-hex-4-ynoic acid 2-((S)-2-tert-butoxycarbonylamino-hex-4-ynoyloxy)benzyl ester 
• 346707-62-8 (S)-2-tert-butoxycarbonylamino-hex-4-ynoic acid 3-((S)-2-tert-butoxycarbonylamino-hex-4-ynoyloxy)benzyl ester 
• 441018-79-7 (S)-2-tert-butoxycarbonylamino-hex-4-ynoic acid 3-hydroxymethylbenzyl ester 
• 346707-86-6 (S)-2-tert-butoxycarbonylamino-hex-4-ynoic acid 2-hydroxymethylbenzyl ester 

Relevant articles and documents

Synthesis of diaminosuberic acid derivatives via ring-closing alkyne metathesis

-