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· · COA & SDS Disponible para cada producto · Envío el mismo día para artículos en stock HexylHIBO - ≥98% , CAS No.334887-43-3
Synonyms
Hexylhomoibotenic acid | DTXSID90398387 | AKOS024456760 | HY-103559 | HEXYLHIBO | alpha-amino-4-hexyl-2,3-dihydro-3-oxo-5-isoxazolepropanoic acid | J-019209 | ?-Amino-4-hexyl-2,3-dihydro-3-oxo-5-isoxazolepropanoic acid | 2-amino-3-(4-hexyl-3-oxo-1,2-oxazo
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Sinónimos
Hexylhomoibotenic acid | DTXSID90398387 | AKOS024456760 | HY-103559 | HEXYLHIBO | alpha-amino-4-hexyl-2,3-dihydro-3-oxo-5-isoxazolepropanoic acid | J-019209 | ?-Amino-4-hexyl-2,3-dihydro-3-oxo-5-isoxazolepropanoic acid | 2-amino-3-(4-hexyl-3-oxo-1,2-oxazo
Especificaciones y pureza
≥98%
Mecanismos bioquímicos y fisiológicos
Group I mGlu receptor antagonist (Kivalues are 140 and 110μM at mGlu1aand mGlu5areceptors respectively). Decreases sEPSCs in rat pyramidal neuronsin vitro.S-enantiomeralso available.
Condiciones de almacenamiento de almacenamiento
Room temperature
Nombres e identificadores Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504762801
Sonrisas canónicas
CCCCCCC1=C(ONC1=O)CC(C(=O)O)N
IUPAC Name
2-amino-3-(4-hexyl-3-oxo-1,2-oxazol-5-yl)propanoic acid
InChIKey
OKJBLHIYOWSQDJ-UHFFFAOYSA-N
INCHI
1S/C12H20N2O4/c1-2-3-4-5-6-8-10(18-14-11(8)15)7-9(13)12(16)17/h9H,2-7,13H2,1H3,(H,14,15)(H,16,17)
Isómeros SMILES
CCCCCCC1=C(ONC1=O)CC(C(=O)O)N
Peso molecular
256.3(free base)
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=43512215&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organic acids and derivatives Clase Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives Direct Parent Alpha amino acids Alternative Parents Aralkylamines Isoxazoles Heteroaromatic compounds Lactams Amino acids Oxacyclic compounds Monocarboxylic acids and derivatives Carboxylic acids Azacyclic compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic heteromonocyclic compounds Substituents Alpha-amino acid - Aralkylamine - Azole - Isoxazole - Heteroaromatic compound - Amino acid - Lactam - Carboxylic acid - Monocarboxylic acid or derivatives - Organoheterocyclic compound - Oxacycle - Azacycle - Organonitrogen compound - Amine - Primary aliphatic amine - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organooxygen compound - Primary amine - Organic oxygen compound - Carbonyl group - Aromatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as alpha amino acids. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon). External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Solubilidad Solvent:1eq. NaOH, Max Conc. mg/mL: 5.13, Max Conc. mM: 20 Peso molecular 256.300 g/mol XLogP3 -0.600 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 8 Exact Mass 256.142 Da Monoisotopic Mass 256.142 Da Topological Polar Surface Area 102.000 Ų Heavy Atom Count 18 Formal Charge 0 Complexity 352.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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