D-allo-Threonine - ≥99% , CAS No.24830-94-2

CAS: 24830-94-2 Cat. No.: T100954 Summenformel: C₄H₉NO₃ Molekulargewicht: 119.12 Beilstein Registry Number: 1721644 EG-Nummer: 246-488-0

QUALITÄT & REINHEIT ≥99%

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)

Storage

Room temperature

Shipped In

Normal

Spezifikationen

Synonyme

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 Show more

Spezifikationen & Reinheit

≥99%

Storage

Room temperature

Verschickt in

Normal

Reinheit

≥99%

Namen und Kennungen

Pubchem Sid

488186633

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488186633

Kanonisches Lächeln

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

Isomere SMILES

C[C@H]([C@H](C(=O)O)N)O

WGK Deutschland

3

RTECS

BA4050000

Molekulargewicht

119.12

Beilstein

1721644

Reaxy-Rn

1098902

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1098902&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Klasse Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Ebene5 Amino acids and derivatives
          • Ebene6 Alpha amino acids and derivatives
            • Ebene7 Alpha amino acids
              • Ebene8 D-alpha-amino acids

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: 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
• Beschreibung: 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.

DOI: 10.1186/s13321-016-0174-y

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Löslichkeit: Soluble in water.
• Spezifische Drehung [α]: [α]D -10° (C=5,H2O)
• Schmelzpunkt (°C): 277-279°C
• Molekulargewicht: 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