CAS 13610-02-1

(2-Propin-1-iloxi)benceno

Descripción:

(2-Propin-1-iloxi)benceno, también conocido como éter fenílico propargílico, es un compuesto orgánico caracterizado por su grupo funcional éter, donde un grupo propargílico está unido a un anillo fenílico. Este compuesto presenta un enlace triple en la parte propargílica, lo que contribuye a su reactividad, particularmente en reacciones relacionadas con alquinos. Típicamente es un líquido incoloro a amarillo pálido con un olor aromático distintivo. La presencia del enlace éter otorga ciertas propiedades de solubilidad, haciéndolo soluble en disolventes orgánicos mientras que es menos soluble en agua. Su estructura química permite aplicaciones potenciales en síntesis orgánica, particularmente en la formación de moléculas más complejas a través de reacciones como sustituciones nucleofílicas o reacciones de acoplamiento. Además, debido a la presencia del grupo alquino, puede participar en reacciones de cicloadición o servir como precursor para varios compuestos funcionalizados. Se deben observar precauciones de seguridad al manipular este compuesto, ya que puede representar riesgos para la salud si se inhala o ingiere.

Fórmula: C₉H₈O

InChI: InChI=1S/C9H8O/c1-2-8-10-9-6-4-3-5-7-9/h1,3-7H,8H2

Clave InChI: InChIKey=AIQRJSXKXVZCJO-UHFFFAOYSA-N

SMILES: O(CC#C)C1=CC=CC=C1

Sinónimos:

• (2-Propyn-1-yloxy)benzene
• (2-Propynyloxy)benzene
• (Phenoxymethyl)acetylene
• (Prop-2-yn-1-yloxy)benzene
• (Propargyloxy)benzene
• 1-(Prop-2-ynyloxy)benzene
• 1-Naphthyl propargyl ether
• 1-Phenoxy-2-propyne
• 2-Propynyoxybenzene
• 3-Phenoxy-1-propyne
• 3-Phenoxypropyne
• 3-Phenyloxy-1-propyne
• Benzene, (2-Propyn-1-Yloxy)-
• Benzene, (2-propynyloxy)-
• Ether, phenyl 2-propynyl
• Phenyl 2-propynyl ether
• Phenyl prop-2-yn-1-yl ether
• Phenyloxymethylacetylene
• Propargyl phenyl ether

Phenyl Propargyl Ether

CAS: 13610-02-1

Fórmula: C₉H₈O

Pureza: >98.0%(GC)

Forma y color: Colorless to Light yellow clear liquid

Peso molecular: 132.16

Ref: 3B-P2222

Phenyl propargyl ether, 98+%

CAS: 13610-02-1

Phenyl propargyl ether is used as an organic chemical synthesis intermediate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or

Fórmula: C₉H₈O

Pureza: 98+%

Forma y color: Clear colorless to yellow to orange, Liquid

Peso molecular: 132.16

Ref: 02-A18272

Phenyl propargyl ether, 97%

CAS: 13610-02-1

Phenyl propargyl ether is used as building block for synthesis. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference

Fórmula: C₉H₈O

Pureza: 97%

Forma y color: Colorless, Liquid

Peso molecular: 132.16

Ref: 02-043923

PHENYL PROPARGYL ETHER

CAS: 13610-02-1

Fórmula: C₉H₈O

Pureza: 97%

Forma y color: Liquid

Peso molecular: 132.1592

Ref: IN-DA003TP9

[(Prop-2-yn-1-yl)oxy]benzene

CAS: 13610-02-1

[(Prop-2-yn-1-yl)oxy]benzene

Pureza: 97%

Forma y color: Colourless To Pale Yellow Liquid

Peso molecular: 132.15922g/mol

Ref: 54-OR25609

Phenylpropargyl ether

CAS: 13610-02-1

Ref: 7W-GW4355

Phenyl propargyl ether

CAS: 13610-02-1

Pureza: 97%

Peso molecular: 132.1620026

Ref: 10-F622645

Phenyl Propargyl Ether

CAS: 13610-02-1

Phenyl propargyl ether (PPE) is a reactive compound that has been used in the synthesis of luminescent probes. PPE reacts with ethyl formate to form an ester and an aldehyde, which can be used for the synthesis of biodiesel. PPE also undergoes nucleophilic attack by deuterium isotope to produce a deuterated product, which is useful in structural biology studies. The reaction mechanism of PPE is similar to that of other organic compounds containing carbon-nitrogen double bonds. NMR spectra show that PPE has a triplet ground state, which is indicative of its reactivity. The activation energies are relatively low, indicating that it is easy to break the covalent bond in the triplet state. This chemical reacts with azides and can be used as a chemical ligation agent for bioconjugation reactions.

Fórmula: C₉H₈O

Pureza: Min. 95%

Peso molecular: 132.16 g/mol

Ref: 3D-NAA61002