[(Phenylmethoxy)methyl]oxirane (Benzyl Glycidyl Ether) - ≥97%(GC) , CAS No.2930-05-4

CAS: 2930-05-4 Cat. No.: P136148 Peso molecular: 164.2 Beilstein Registry Number: 17(5)3,16 Número EC: 220-899-5

GRADE & PURITY ≥97%(GC)

Synonyms

(S)-(+)-Glycidyl Benzyl Ether | [(Phenylmethoxy)methyl]oxirane | 1-(Benzyloxy)-2,3-epoxypropane | 3-(Benzyloxy)-1,2-epoxypropane | 2-[[(Benzyloxy)methyl]oxy]oxirane | 2-[(Phenylmethoxy)methyl]oxirane | (±)-O-Benzylglycidol | Benzyloxymethyl)oxirane

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Specifications

Sinónimos

(S)-(+)-Glycidyl Benzyl Ether | [(Phenylmethoxy)methyl]oxirane | 1-(Benzyloxy)-2, 3-epoxypropane | 3-(Benzyloxy)-1, 2-epoxypropane | 2-[[(Benzyloxy)methyl]oxy]oxirane | 2-[(Phenylmethoxy)methyl]oxirane | (±)-O-Benzylglycidol | Benzyloxymethyl)oxirane

Especificaciones y pureza

≥97%(GC)

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%(GC)

Nombres e identificadores

• Pubchem Sid: 504756209
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504756209
• Sonrisas canónicas: C1C(O1)COCC2=CC=CC=C2
• IUPAC Name: 2-(phenylmethoxymethyl)oxirane
• InChIKey: QNYBOILAKBSWFG-UHFFFAOYSA-N
• INCHI: 1S/C10H12O2/c1-2-4-9(5-3-1)6-11-7-10-8-12-10/h1-5,10H,6-8H2
• Isómeros SMILES: C1C(O1)COCC2=CC=CC=C2
• RTECS: TX2860000
• Peso molecular: 164.2
• Beilstein: 17(5)3,16
• Reaxy-Rn: 115279
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=115279&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Benzylethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzylethers
• Alternative Parents: Oxacyclic compounds Epoxides Dialkyl ethers Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Benzylether - Oxacycle - Organoheterocyclic compound - Ether - Oxirane - Dialkyl ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as benzylethers. These are aromatic ethers with the general formula ROCR' (R = alkyl, aryl; R'=benzene).
• 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: Air Sensitive,Heat Sensitive
• Índice de refracción: 1.52
• Punto de inflamación (°F): 235.4 °F
• Punto de inflamación (°C): 113 °C
• Punto de ebullición (°C): 75 °C/11 mmHg
• Peso molecular: 164.200 g/mol
• XLogP3: 1.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 164.084 Da
• Monoisotopic Mass: 164.084 Da
• Topological Polar Surface Area: 21.800 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 130.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• 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. Yi Liu, Shuangjiang Li, Xiaojian Yu, Ying Chen, Xiaoning Tang, Tianding Hu, Lan Shi, Manoj Pudukudy, Shaoyun Shan, Yunfei Zhi.  (2023)  Cellulose nanofibers (CNF) supported (Salen)Cr(III) composite as an efficient heterogeneous catalyst for CO2 cycloaddition.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2023.113344]

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