Éter metílico de trifluoreto de boro - ≥60% , CAS No.353-42-4

CAS: 353-42-4 Cat. No.: B119885 Fórmula: C₂H₆0BF₃ Peso molecular: 113.87 Beilstein Registry Number: 3613739 Número CE: 206-532-1 PubChem CID: 2724165

GRADE & PURITY ≥60%

Synonyms

trifluoroborato de (dimetiloxónio) | Boranueto de dimetiloxónio (trifluoro) | Éter metílico de trifluoreto de boro | MFCD00013192 | FT-0632018 | Éter dimetílico de trifluoreto de boro | FOWZWMGLMYVYDH-UHFFFAOYSA-N | AKOS015916108

Storage

Argon charged,Room temperature

Shipped In

FedEx DG Service

Visão geral

Reactante ou reagente envolvido em: Deconvolução da cinética da reação química de troca de ligandos platina-prata Síntese do gangliosídeo neurogénico LLG-3 da estrela do mar através de reacções de glicosilação Síntese da pelorusida através de lactonização e rela

Specifications

Sinónimos

trifluoroborato de (dimetiloxónio) | Boranueto de dimetiloxónio (trifluoro) | Éter metílico de trifluoreto de boro | MFCD00013192 | FT-0632018 | Éter dimetílico de trifluoreto de boro | FOWZWMGLMYVYDH-UHFFFAOYSA-N | AKOS015916108

Especificações e pureza

≥60%

Condições de armazenamento de armazenamento

Argon charged,Room temperature

Enviado em

FedEx DG Service

Pureza

≥60%

Nomes e identificadores

Pubchem Sid

508811501

Sorrisos canónicos

B(F)(F)F.COC

IUPAC Name

methoxymethane;trifluoroborane

InChIKey

KTPWETRNSUKEME-UHFFFAOYSA-N

INCHI

1S/C2H6O.BF3/c1-3-2;2-1(3)4/h1-2H3;

SMILES isoméricas

B(F)(F)F.COC

WGK Alemanha

3

RTECS

ED8400000

PubChem CID

2724165

Número UN

2965

Grupo de embalagem

I

Peso molecular

113.87

Beilstein

3613739

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: 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
• Descrição: 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

Propriedades químicas e físicas

• Sensibilidade: Moisture sensitive
• Ponto de inflamação (°F): 143.6 °F
• Ponto de inflamação (°C): 62 °C
• Ponto de ebulição (°C): 126-127°C
• Ponto de fusão (°C): -15°C
• Peso molecular: 113.880 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 114.046 Da
• Monoisotopic Mass: 114.046 Da
• Topological Polar Surface Area: 9.200 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 24.100
• 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

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