1-Aminocyclobutanecarboxylic Acid Hydrochloride
1-Aminocyclobutanecarboxylic Acid Hydrochloride Basic information
- Product Name:
- 1-Aminocyclobutanecarboxylic Acid Hydrochloride
- Synonyms:
-
- AMino-1-cyclobutanecarboxylic acid hydrochloride
- 1-aMino-
- 1-AMinocyclobutane
- 1-aMinocyclobutane-1-carboxylic acid hydrochloride
- 1-AminocyclobutanecarboxylicAcidHydrochloride,98%
- 1-AminocyclobutanecarboxlicacidHCl
- 1-Aminocyclobutanecarboxlicacidmonohydrochloride
- 1-AMINO CYCLOBUTANE CARBOXYLIC ACID HYDROCHLORIDE
- CAS:
- 98071-16-0
- MF:
- C5H10ClNO2
- MW:
- 151.5914
- EINECS:
- 619-316-0
- Product Categories:
-
- Cyclobutanes & Cyclobutenes
- Simple 4-Membered Ring Compounds
- 1
- Mol File:
- 98071-16-0.mol
1-Aminocyclobutanecarboxylic Acid Hydrochloride Chemical Properties
- Melting point:
- 226 °C
- RTECS
- GU1336000
- storage temp.
- Inert atmosphere,2-8°C
- Water Solubility
- Soluble in water
- form
- Powder
- color
- White to Almost white
- InChI
- InChI=1S/C5H9NO2.ClH/c6-5(4(7)8)2-1-3-5;/h1-3,6H2,(H,7,8);1H
- InChIKey
- HBTVGNDTGRUBQO-UHFFFAOYSA-N
- SMILES
- C1(N)(C(O)=O)CCC1.[H]Cl
1-Aminocyclobutanecarboxylic Acid Hydrochloride Usage And Synthesis
Uses
NMDA receptor antagonist acting at the glycine site
Application
1-Aminocyclobutanecarboxylic Acid Hydrochloride is an essential organic synthesis reagent with good chemical stability and ease of use. It is widely used in organic synthesis and medicinal chemistry, helping to prepare complex organic molecules, including peptide chains, drugs, and four-membered ring bioactive molecules. This substance can be used in synthesizing polypeptides and can be used to activate amino acids to form peptide bonds. It is widely used in pharmaceutical synthesis to synthesize drug intermediates, especially drug molecules containing amino acid residues. It can be used to construct the skeleton structure of biologically active molecules.
Synthesis
Ethyl 1-aminocyclobutanecarboxylate (1.0 g, 6.28 mmol) was dissolved in 1N HCl (10 ml) in a dry reaction flask and the resulting reaction mixture was heated to reflux and stirred at reflux for about 2 hours. The progress of the reaction was monitored by TLC spot plate and at the end of the reaction the reaction mixture was concentrated directly to dryness under vacuum to give the target product molecule 1-amino-1-cyclobutanecarboxylic acid hydrochloride, which can be further purified by recrystallization if necessary.
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