2-Deoxy-D-ribose - BioReagent, for Cell culture, Moligand™, 10wt. % in medium chain triglycerides (MCTG) , CAS No.533-67-5

CAS: 533-67-5 Cat. No.: D485294 Fórmula: C₅H₁₀O₄ Peso molecular: 134.13 Beilstein Registry Number: 1721978 Número CE: 208-573-0

GRADE & PURITY BioReagent, Moligand™, for Cell culture, 10wt. % in medium chain triglycerides (MCTG)

Synonyms

2-Deoxy-D-ribose, 97% | CHEBI:28816 | NSC-772796 | ASJSAQIRZKANQN-CRCLSJGQSA-N | BBL012499 | 2-Deoxy-D-ribose | 2-Deoxy-D-ribose, >=99.0% (TLC) | AM20100306 | 4-01-00-04181 (Beilstein Handbook Reference) | aldehydo-2-deoxy-D-ribose | D-erythro-Pentose, 2-

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Sinónimos

2-Deoxy-D-ribose, 97% | CHEBI:28816 | NSC-772796 | ASJSAQIRZKANQN-CRCLSJGQSA-N | BBL012499 | 2-Deoxy-D-ribose | 2-Deoxy-D-ribose, >=99.0% (TLC) | AM20100306 | 4-01-00-04181 (Beilstein Handbook Reference) | aldehydo-2-deoxy-D-ribose | D-erythro-Pentose, 2-

Especificações e pureza

BioReagent, for Cell culture, Moligand™, 10wt. % in medium chain triglycerides (MCTG)

Condições de armazenamento de armazenamento

Store at 2-8°C

Enviado em

Wet ice

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Grau

BioReagent, for Cell culture, Moligand™

Nomes e identificadores

Pubchem Sid

504763826

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504763826

Sorrisos canónicos

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

IUPAC Name

(3S,4R)-3,4,5-trihydroxypentanal

InChIKey

ASJSAQIRZKANQN-CRCLSJGQSA-N

INCHI

1S/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m0/s1

SMILES isoméricas

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

WGK Alemanha

3

RTECS

SB7230000

Peso molecular

134.13

Beilstein

1721978

Reaxy-Rn

1904591

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1904591&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Carbonyl compounds
        • Level5 Aldehydes
          • Level6 Beta-hydroxy aldehydes

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbonyl compounds
• Intermediate Tree Nodes: Aldehydes
• Direct Parent: Beta-hydroxy aldehydes
• Alternative Parents: Alpha-hydrogen aldehydes Secondary alcohols Polyols Short-chain aldehydes Primary alcohols Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Beta-hydroxy aldehyde - Alpha-hydrogen aldehyde - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Short-chain aldehyde - Primary alcohol - Alcohol - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as beta-hydroxy aldehydes. These are organic compounds containing an aldehyde substituted with a hydroxy group on the second carbon atom.
• External Descriptors: deoxypentose

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

Propriedades químicas e físicas

• Solubilidade: water: 100mg/mL, clear to slightly hazy, colorless to light yellow
• Rotação específica [α]: -56 ° (C=1, H2O)
• Ponto de fusão (°C): 91°C
• Peso molecular: 134.130 g/mol
• XLogP3: -2.300
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 134.058 Da
• Monoisotopic Mass: 134.058 Da
• Topological Polar Surface Area: 77.800 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 83.000
• 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