Boron trifluoride diethyl etherate - Distillation grade, ≥46.5% BF3 basis , CAS No.109-63-7

CAS: 109-63-7 Cat. No.: B431394 Fórmula: C₄H₁₀BF₃O Peso molecular: 141.93 Beilstein Registry Number: 3909607 Número EC: 203-689-8 PubChem CID: 8000

GRADE & PURITY Distillation grade, ≥46.5% BF3 basis

Synonyms

boron trifluorideetherate | boron trifluoride-etherate | boron trifloride etherate | ethoxyethane;trifluoroborane | diethyl ether trifluoroborane | borontriflouride etherate | borontrifluoride etherate | BF3 OEt2 | DTXSID601015537 | A802065 | Ethyl ether,

Storage

Store at 2-8°C,Argon charged,Desiccated

Shipped In

Wet ice,FedEx DG Service

Descripción general

Application

Catalyst in the synthesis of polyol chains. Reagent for the coupling of imines to allylstannanes and 4′-nitrobenzenesulfenanilide to alkenes and alkynes.

Specifications

Sinónimos

boron trifluorideetherate | boron trifluoride-etherate | boron trifloride etherate | ethoxyethane;trifluoroborane | diethyl ether trifluoroborane | borontriflouride etherate | borontrifluoride etherate | BF3 OEt2 | DTXSID601015537 | A802065 | Ethyl ether,

Especificaciones y pureza

Distillation grade, ≥46.5% BF3 basis

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C,Argon charged,Desiccated

Enviado en

Wet ice,FedEx DG Service

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

Grado

Distillation grade

Nombres e identificadores

Pubchem Sid

508811500

Sonrisas canónicas

B(F)(F)F.CCOCC

IUPAC Name

ethoxyethane;trifluoroborane

InChIKey

KZMGYPLQYOPHEL-UHFFFAOYSA-N

INCHI

1S/C4H10O.BF3/c1-3-5-4-2;2-1(3)4/h3-4H2,1-2H3;

Isómeros SMILES

B(F)(F)F.CCOCC

WGK Alemania

1

PubChem CID

8000

Número ONU

2604

Grupo de embalaje

I

Peso molecular

141.93

Beilstein

3909607

Reaxy-Rn

3909607

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Ethers

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Ethers
• Intermediate Tree Nodes: Not available
• Direct Parent: Dialkyl ethers
• Alternative Parents: Organic metalloid salts Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organic metalloid salt - Dialkyl ether - Hydrocarbon derivative - Organic salt - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as dialkyl ethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are alkyl groups.
• 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；Hygroscopic
• Índice de refracción: 1.348
• Punto de inflamación (°F): 137.3 °F - closed cup
• Punto de inflamación (°C): <22℃
• Punto de ebullición (°C): 125.7°C
• Punto de fusión (°C): -60.4°C
• Peso molecular: 141.930 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 142.078 Da
• Monoisotopic Mass: 142.078 Da
• Topological Polar Surface Area: 9.200 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 19.100
• 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: 2

XLogP3