Tri-o-tolyl Phosphite - ≥97% , CAS No.2622-08-4

CAS: 2622-08-4 Cat. No.: T161946 Peso molecular: 352.37 Número EC: 220-068-7 PubChem CID: 92937

GRADE & PURITY ≥97%

Synonyms

Carprost | AS-66177 | N-(3,4-Dimethoxycinnamoyl)anthranilic acid | Tri-o-cresyl phosphite | tri(2-methylphenyl)phosphite | tri(o-tolyl)phosphite | Tris(2-methylphenyl) phosphite # | Tris(o-methylphenyl) phosphite | CHEBI:34727 | Phosphorous acid, tri-o-cr

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Descripción general

application：

Tri(o-tolyl) phosphite is used as a plasticizer and in organic synthesis.

Specifications

Sinónimos

Carprost | AS-66177 | N-(3, 4-Dimethoxycinnamoyl)anthranilic acid | Tri-o-cresyl phosphite | tri(2-methylphenyl)phosphite | tri(o-tolyl)phosphite | Tris(2-methylphenyl) phosphite # | Tris(o-methylphenyl) phosphite | CHEBI:34727 | Phosphorous acid, tri-o-cr

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Argon charged

Enviado en

Wet ice

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

Pureza

≥97%

Nombres e identificadores

• Pubchem Sid: 504756152
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504756152
• Sonrisas canónicas: CC1=CC=CC=C1OP(OC2=CC=CC=C2C)OC3=CC=CC=C3C
• IUPAC Name: tris(2-methylphenyl) phosphite
• InChIKey: BKHZQJRTFNFCTG-UHFFFAOYSA-N
• INCHI: 1S/C21H21O3P/c1-16-10-4-7-13-19(16)22-25(23-20-14-8-5-11-17(20)2)24-21-15-9-6-12-18(21)3/h4-15H,1-3H3
• Isómeros SMILES: CC1=CC=CC=C1OP(OC2=CC=CC=C2C)OC3=CC=CC=C3C
• RTECS: TH1050000
• PubChem CID: 92937
• Peso molecular: 352.37
• Reaxy-Rn: 1892738

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Phenoxy compounds

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Phenoxy compounds
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenoxy compounds
• Alternative Parents: Toluenes Organic phosphites Organooxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenoxy compound - Toluene - Organic phosphite - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenoxy compounds. These are aromatic compounds contaning a phenoxy group.
• 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

• Solubilidad: Not miscible or difficult to mix in water.
• Sensibilidad: Sensitive to air; sensitive to humidity; sensitive to heat
• Índice de refracción: 1.58
• Punto de ebullición (°C): 238 °C/11 mmHg
• Peso molecular: 352.400 g/mol
• XLogP3: 6.600
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 6
• Exact Mass: 352.123 Da
• Monoisotopic Mass: 352.123 Da
• Topological Polar Surface Area: 27.700 Ų
• Heavy Atom Count: 25
• Formal Charge: 0
• Complexity: 334.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• 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