CAS 13610-02-1

(2-Propin-1-ilossi)benzene

Descrizione:

(2-Propin-1-ilossi)benzene, noto anche come etere fenilico propargilico, è un composto organico caratterizzato dal suo gruppo funzionale etere, dove un gruppo propargilico è attaccato a un anello fenilico. Questo composto presenta un legame triplo nella parte propargilica, che contribuisce alla sua reattività, in particolare nelle reazioni legate agli alchini. È tipicamente un liquido incolore o giallo pallido con un odore aromatico distintivo. La presenza del legame etere conferisce determinate proprietà di solubilità, rendendolo solubile in solventi organici mentre è meno solubile in acqua. La sua struttura chimica consente potenziali applicazioni nella sintesi organica, in particolare nella formazione di molecole più complesse attraverso reazioni come sostituzioni nucleofile o reazioni di accoppiamento. Inoltre, a causa della presenza del gruppo alchino, può partecipare a reazioni di cicloaddizione o fungere da precursore per vari composti funzionalizzati. Devono essere osservate precauzioni di sicurezza quando si maneggia questo composto, poiché può comportare rischi per la salute se inalato o ingerito.

Formula: C₉H₈O

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

InChI key: InChIKey=AIQRJSXKXVZCJO-UHFFFAOYSA-N

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

Sinonimi:

• (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

Formula: C₉H₈O

Purezza: >98.0%(GC)

Colore e forma: Colorless to Light yellow clear liquid

Peso molecolare: 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

Formula: C₉H₈O

Purezza: 98+%

Colore e forma: Clear colorless to yellow to orange, Liquid

Peso molecolare: 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

Formula: C₉H₈O

Purezza: 97%

Colore e forma: Colorless, Liquid

Peso molecolare: 132.16

Ref: 02-043923

PHENYL PROPARGYL ETHER

CAS: 13610-02-1

Formula: C₉H₈O

Purezza: 97%

Colore e forma: Liquid

Peso molecolare: 132.1592

Ref: IN-DA003TP9

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

CAS: 13610-02-1

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

Purezza: 97%

Colore e forma: Colourless To Pale Yellow Liquid

Peso molecolare: 132.15922g/mol

Ref: 54-OR25609

Phenylpropargyl ether

CAS: 13610-02-1

Ref: 7W-GW4355

Phenyl propargyl ether

CAS: 13610-02-1

Purezza: 97%

Peso molecolare: 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.

Formula: C₉H₈O

Purezza: Min. 95%

Peso molecolare: 132.16 g/mol

Ref: 3D-NAA61002