(S)-(+)-1,2-Isopropylideneglycerol - ≥98%(GC) , CAS No.22323-82-6

CAS: 22323-82-6 Cat. No.: I123573 Peso molecular: 132.16 Beilstein Registry Number: 80118 Número EC: 244-910-8

GRADE & PURITY ≥98%(GC)

Synonyms

1,3-Dioxolane-4-methanol, 2,2-dimethyl-, (4S)- | [(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]methanol;(S)-(+)-2,2-Dimethyl-1,3-dioxolane-4-methanol | 1,3-Dioxolane-4-methanol, 2,2-dimethyl-, (S)- | s-glycerol acetonide | F11426 | (S)-(+)-(2,2-dimethyl-[1,3]dioxo

Storage

Room temperature

Shipped In

Normal

Descripción general

(S)-(+)-1,2-Isopropylideneglycerol is used in a synthesis of a chiral allylic triol via extrusion of SO2 from an α,β-epoxysulfone. (S)-(+)-2,3-O-Isopropylideneglycerol is an inhibitor of MEK.
A biochemical used in a synthesis of a chiral allylic triol

Specifications

Sinónimos

1, 3-Dioxolane-4-methanol, 2, 2-dimethyl-, (4S)- | [(4S)-2, 2-dimethyl-1, 3-dioxolan-4-yl]methanol;(S)-(+)-2, 2-Dimethyl-1, 3-dioxolane-4-methanol | 1, 3-Dioxolane-4-methanol, 2, 2-dimethyl-, (S)- | s-glycerol acetonide | F11426 | (S)-(+)-(2, 2-dimethyl-[1, 3]dioxo

Especificaciones y pureza

≥98%(GC)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%(GC)

Nombres e identificadores

• Pubchem Sid: 488191325
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488191325
• Sonrisas canónicas: CC1(OCC(O1)CO)C
• IUPAC Name: [(4S)-2,2-dimethyl-1,3-dioxolan-4-yl]methanol
• InChIKey: RNVYQYLELCKWAN-YFKPBYRVSA-N
• INCHI: 1S/C6H12O3/c1-6(2)8-4-5(3-7)9-6/h5,7H,3-4H2,1-2H3/t5-/m0/s1
• Isómeros SMILES: CC1(OC[C@@H](O1)CO)C
• WGK Alemania: 1
• Peso molecular: 132.16
• Beilstein: 80118
• Reaxy-Rn: 80119
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=80119&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Ethers
        • Level5 Acetals
          • Level6 Ketals

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Ethers
• Intermediate Tree Nodes: Acetals
• Direct Parent: Ketals
• Alternative Parents: 1,3-dioxolanes Oxacyclic compounds Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Ketal - Meta-dioxolane - Oxacycle - Organoheterocyclic compound - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as ketals. These are acetals derived from ketones by replacement of the oxo group by two hydrocarbyloxy groups R2C(OR)2 ( R not Hydrogen ). This term, once abandoned, has been reinstated as a subclass of acetals.
• 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

• Sensibilidad: Hygroscopic
• Índice de refracción: 1.435
• Rotación específica [α]: +11.5°C(c=5 in methanol)
• Punto de inflamación (°F): 194 °F
• Punto de inflamación (°C): 80°(176°F)
• Punto de ebullición (°C): 82-83°/14mmHg
• Peso molecular: 132.160 g/mol
• XLogP3: -0.200
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 132.079 Da
• Monoisotopic Mass: 132.079 Da
• Topological Polar Surface Area: 38.700 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 100.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• 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