Glycolaldehyde dimer - Reagent grade , CAS No.23147-58-2

CAS: 23147-58-2 Cat. No.: G168832 Peso molecular: 120.1 Beilstein Registry Number: 506029 Número EC: 607-202-3

GRADE & PURITY Reagent Grade

Synonyms

[1,4]-dioxan-2,5-diol | EINECS 204-590-2 | DTXSID60945822 | JNG39F464R | Glycoaldehyde dimer | 1,4-Dioxane-2,5-diol # | 14-Dioxane-25-diol | D92592 | SCHEMBL52731 | 2,5-DIHYDROXY-P-DIOXANE | FT-0602682 | s3334 | 1,4-Dioxane-2,5-diol | AM20090246 | EN300-8

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Sinónimos

[1, 4]-dioxan-2, 5-diol | EINECS 204-590-2 | DTXSID60945822 | JNG39F464R | Glycoaldehyde dimer | 1, 4-Dioxane-2, 5-diol # | 14-Dioxane-25-diol | D92592 | SCHEMBL52731 | 2, 5-DIHYDROXY-P-DIOXANE | FT-0602682 | s3334 | 1, 4-Dioxane-2, 5-diol | AM20090246 | EN300-8

Especificaciones y pureza

Reagent grade

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Grado

Reagent Grade

Nombres e identificadores

• Pubchem Sid: 504757736
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504757736
• Sonrisas canónicas: C1C(OCC(O1)O)O
• IUPAC Name: 1,4-dioxane-2,5-diol
• InChIKey: ATFVTAOSZBVGHC-UHFFFAOYSA-N
• INCHI: 1S/C4H8O4/c5-3-1-7-4(6)2-8-3/h3-6H,1-2H2
• Isómeros SMILES: C1C(OCC(O1)O)O
• WGK Alemania: 3
• Peso molecular: 120.1
• Beilstein: 506029
• Reaxy-Rn: 104399
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=104399&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Dioxanes
      • Subclass 1,4-dioxanes

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Dioxanes
• Subclass: 1,4-dioxanes
• Intermediate Tree Nodes: Not available
• Direct Parent: 1,4-dioxanes
• Alternative Parents: Hemiacetals Oxacyclic compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Para-dioxane - Hemiacetal - Oxacycle - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as 1,4-dioxanes. These are organic compounds containing 1,4-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 4.
• 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.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Peso molecular: 120.100 g/mol
• XLogP3: -1.300
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 120.042 Da
• Monoisotopic Mass: 120.042 Da
• Topological Polar Surface Area: 58.900 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 64.400
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 2
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

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2. Muge Niu, Yucui Hou, Weize Wu, Shuhang Ren, Ru Yang.  (2018)  Successive C1–C2 bond cleavage: the mechanism of vanadium(V)-catalyzed aerobic oxidation of D-glucose to formic acid in aqueous solution.  PHYSICAL CHEMISTRY CHEMICAL PHYSICS,  20  (26): (17942-17951).  [PMID:29926044] [10.1039/C8CP02352B]

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6. Kong Linghong, Wang Hui, Jiang Weiwei, Chen Yun, Du Zhuoling, Zhang Qiong, Dong Jianyue, Zeng Changchun, Liu Hanping.  (2025)  Network pharmacology-based study in polymetformin’s new function of blocking ages/rage pathway curing diabetic complications.  Scientific Reports,  15  (1): (1-11).  [PMID:40467581] [10.1038/s41598-025-00956-w]

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