L-Talose - ≥98%(HPLC) , CAS No.23567-25-1

CAS: 23567-25-1 Cat. No.: L130880 Formule: C₆H₁₂O₆ Poids moléculaire: 180.16

QUALITÉ & PURETÉ ≥98%(HPLC)

Synonyms

(2R,3R,4R,5S)-2,3,4,5,6-pentahydroxyhexanal | aldehydo-L-talose | DTXSID701319160 | T1767 | AS-56035 | FT-0624556 | SCHEMBL16164349 | GEO-04669 | A878210 | EINECS 245-744-9 | L-Talose | W-201988 | AKOS027320154 | D92524 | Q27158868 | HY-W145580 | L-(-)-TA

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Spécifications

Synonymes

(2R,3R,4R,5S)-2,3,4,5,6-pentahydroxyhexanal | aldehydo-L-talose | DTXSID701319160 | T1767 | AS-56035 | FT-0624556 | SCHEMBL16164349 | GEO-04669 | A878210 | EINECS 245-744-9 | L-Talose | W-201988 | AKOS027320154 | D92524 | Q27158868 | HY-W145580 | L-(-)-TA

Spécifications et pureté

≥98%(HPLC)

Conditions de stockage de stockage

Store at 2-8°C,Argon charged

Expédié en

Wet ice

Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.

Pureté

≥98%(HPLC)

Noms et identifiants

Pubchem Sid

488186600

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488186600

Sourires canoniques

C(C(C(C(C(C=O)O)O)O)O)O

IUPAC Name

(2R,3R,4R,5S)-2,3,4,5,6-pentahydroxyhexanal

InChIKey

GZCGUPFRVQAUEE-OMMKOOBNSA-N

INCHI

1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h1,3-6,8-12H,2H2/t3-,4-,5-,6+/m0/s1

Isomères SMILES

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

Poids moléculaire

180.16

Reaxy-Rn

1908976

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1908976&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Monosaccharides
          • Level6 Hexoses

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Monosaccharides
• Direct Parent: Hexoses
• Alternative Parents: Medium-chain aldehydes Beta-hydroxy aldehydes Alpha-hydroxyaldehydes Secondary alcohols Polyols Primary alcohols Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hexose monosaccharide - Medium-chain aldehyde - Beta-hydroxy aldehyde - Alpha-hydroxyaldehyde - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Primary alcohol - Carbonyl group - Aldehyde - Alcohol - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as hexoses. These are monosaccharides in which the sugar unit is a is a six-carbon containing moeity.
• External Descriptors: L-talose

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

Propriétés chimiques et physiques

• Sensibilité: Moisture sensitive
• Rotation spécifique [α]: -20° (C=1,H2O)
• Point de fusion (°C): 133 °C
• Poids moléculaire: 180.160 g/mol
• XLogP3: -2.900
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 5
• Exact Mass: 180.063 Da
• Monoisotopic Mass: 180.063 Da
• Topological Polar Surface Area: 118.000 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 138.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 4
• 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