Benzyl (S)-(+)-glycidyl ether - ≥98%(GC) , CAS No.16495-13-9

CAS: 16495-13-9 Cat. No.: B119630 Peso molecular: 164.2 Beilstein Registry Number: 5246495 Número EC: 605-380-7

GRADE & PURITY ≥98%(GC)

Synonyms

(S)-2-(benzyloxymethyl)oxirane | (S)-benzylglycidyl ether | (S)-benzyloxymethyloxirane | (S)-Benzyloxymethyl-oxirane | O-benzyl-glycidol | (S)-O-Benzylglycidol | Z1255431172 | Benzyl-(S)-(+)-glycidyl ether | Benzyl(S)-(+)-glycidyl ether | Propane, 1-(benz

Storage

Room temperature

Shipped In

Normal

Descripción general

Product Application：

(S)-(+)-Glycidyl benzyl ether can be used to prepare 1-octadecyl-3-O-benzyl-sn-glycerol, which is a key intermediate for the synthesis of triglycerides containing α-eleostearic acid.

Specifications

Sinónimos

(S)-2-(benzyloxymethyl)oxirane | (S)-benzylglycidyl ether | (S)-benzyloxymethyloxirane | (S)-Benzyloxymethyl-oxirane | O-benzyl-glycidol | (S)-O-Benzylglycidol | Z1255431172 | Benzyl-(S)-(+)-glycidyl ether | Benzyl(S)-(+)-glycidyl ether | Propane, 1-(benz

Especificaciones y pureza

≥98%(GC)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%(GC)

Nombres e identificadores

• Pubchem Sid: 504757299
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504757299
• Sonrisas canónicas: C1C(O1)COCC2=CC=CC=C2
• IUPAC Name: (2S)-2-(phenylmethoxymethyl)oxirane
• InChIKey: QNYBOILAKBSWFG-SNVBAGLBSA-N
• INCHI: 1S/C10H12O2/c1-2-4-9(5-3-1)6-11-7-10-8-12-10/h1-5,10H,6-8H2/t10-/m1/s1
• Isómeros SMILES: C1[C@H](O1)COCC2=CC=CC=C2
• WGK Alemania: 3
• RTECS: TX2860030
• Peso molecular: 164.2
• Beilstein: 5246495
• 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

• Índice de refracción: 1.517
• Rotación específica [α]: 16° (neat)
• Punto de inflamación (°F): >110°
• Punto de inflamación (°C): >110°
• Punto de ebullición (°C): 130°C
• 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: 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

Referencias

1. Xiaotong Fu, Meili Ding, Yang Wang, Jiani Chen, Jianfeng Yao.  (2025)  An etching-coordination strategy to construct yolk–shell structured ZIF/Fe–tannic acid composites for enhancing photothermal catalytic CO2 cycloaddition.  Journal of Materials Chemistry A,      [PMID:] [10.1039/D5TA07312J]