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· · COA & SDS Disponibile per ogni prodotto · Spedizione lo stesso giorno su articoli in magazzino D-allo-Threonine - ≥99% , CAS No.24830-94-2
Synonyms
allo-D-threonine|H-D-ALLO-THR-OH|Allothreonine, D-|D(-)-allo-Threonine|(2R,3R)-2-amino-3-hydroxybutanoic acid|(2R3R)-2-Amino-3-hydroxybutyric acid|(2R,3R)-2-azaniumyl-3-hydroxy-butanoate;D-allo-Threonine|cis-Vinylenebis(diphenylphosphine)|D-Allothreonine|D-allo-Threonine|DL-allothreonine|DL-allo-Threonine|Threonine, allo-|(2R,3R)-3-HYDROXY-2-AMINOBUTANOIC ACID|(R)-Allothreonine|FB1|(2R,3R)-Allothreonine|1,3-Benzenediamine,N1,N1-dimethyl-4-nitro-|(2R,3R)-2-amino-3-hydroxybutanoicacid|D-allo-Thr|(2S)-2-acetamido-N-[(2S)-1-[[(2S)-5-(diaminomethylideneamino)-1-oxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]-4-methylpentanamide;sulfuric acid|DL-ALLOTHREONINE (CONTAINS THREONINE)
Specifiche Sinonimi
allo-D-threonine | H-D-ALLO-THR-OH | Allothreonine, D- | D(-)-allo-Threonine | (2R,3R)-2-amino-3-hydroxybutanoic acid | (2R3R)-2-Amino-3-hydroxybutyric acid | (2R,3R)-2-azaniumyl-3-hydroxy-butanoate;D-allo-Threonine | cis-Vinylenebis(diphenylphosphine) | D-Allothreonine | D-allo-Threonine | DL-allothreonine | DL-allo-Threonine | Threonine Mostra altro
Condizioni di conservazione di stoccaggio
Room temperature
Nomi e identificatori Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488186633
Sorrisi canonici
CC(C(C(=O)O)N)O
IUPAC Name
(2R,3R)-2-amino-3-hydroxybutanoic acid
InChIKey
AYFVYJQAPQTCCC-PWNYCUMCSA-N
INCHI
1S/C4H9NO3/c1-2(6)3(5)4(7)8/h2-3,6H,5H2,1H3,(H,7,8)/t2-,3-/m1/s1
Isomeri SMILES
C[C@H]([C@H](C(=O)O)N)O
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1098902&ln=
Dati avanzati Taxonomic Classification Kingdom Organic compounds Superclass Organic acids and derivatives Classe Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives - Alpha amino acids Direct Parent D-alpha-amino acids Alternative Parents Short-chain hydroxy acids and derivatives Beta hydroxy acids and derivatives Fatty acids and conjugates Secondary alcohols Amino acids Monocarboxylic acids and derivatives Carboxylic acids Organopnictogen compounds Organic oxides Monoalkylamines Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aliphatic acyclic compounds Substituents D-alpha-amino acid - Beta-hydroxy acid - Short-chain hydroxy acid - Hydroxy acid - Fatty acid - Amino acid - Secondary alcohol - Carboxylic acid - Monocarboxylic acid or derivatives - Alcohol - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Organic oxide - Primary aliphatic amine - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Amine - Aliphatic acyclic compound Descrizione This compound belongs to the class of organic compounds known as d-alpha-amino acids. These are alpha amino acids which have the D-configuration of the alpha-carbon atom. External Descriptors allothreonine 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.
Struttura 3D Obiettivi associati (non umani) Meccanismi d'azione Certificati (CoA, COO, BSE/TSE e tabella di analisi) Proprietà chimiche e fisiche Solubilità Soluble in water. Rotazione specifica [α] [α]D -10° (C=5,H2O) Punto di fusione (°C) 277-279°C Peso molecolare 119.120 g/mol XLogP3 -2.900 Hydrogen Bond Donor Count 3 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 2 Exact Mass 119.058 Da Monoisotopic Mass 119.058 Da Topological Polar Surface Area 83.600 Ų Heavy Atom Count 8 Formal Charge 0 Complexity 93.300 Isotope Atom Count 0 Defined Atom Stereocenter Count 2 Undefined Atom Stereocenter Count 0 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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