CAS 464-07-3

3,3-Dimetil-2-butanolo

Descrizione:

3,3-Dimetil-2-butanolo è un alcol a catena ramificata caratterizzato dalla sua formula molecolare C₆H₁₄O. Presenta un gruppo funzionale idrossile (-OH) attaccato a un atomo di carbonio che è anche connesso a due gruppi metilici, rendendolo un alcol terziario. Questa struttura contribuisce alle sue uniche proprietà fisiche e chimiche. Il composto è tipicamente un liquido incolore con un odore caratteristico ed è solubile in solventi organici, ma ha una solubilità limitata in acqua a causa delle sue catene idrocarburiche idrofobiche. Il suo punto di ebollizione è relativamente alto rispetto agli alcoli a catena lineare, riflettendo l'influenza dell'ostruzione sterica dei gruppi metilici. 3,3-Dimetil-2-butanolo può partecipare a varie reazioni chimiche, tra cui disidratazione e ossidazione, rendendolo utile nella sintesi organica. Inoltre, è impiegato nella produzione di fragranze e come solvente in varie applicazioni industriali. I dati di sicurezza indicano che deve essere maneggiato con cura, poiché può essere infiammabile e può causare irritazione al contatto con la pelle o gli occhi.

Formula: C₆H₁₄O

InChI: InChI=1S/C6H14O/c1-5(7)6(2,3)4/h5,7H,1-4H3

InChI key: InChIKey=DFOXKPDFWGNLJU-UHFFFAOYSA-N

SMILES: C(C(C)O)(C)(C)C

Sinonimi:

• (2R)-3,3-dimethylbutan-2-ol
• (2S)-3,3-dimethylbutan-2-ol
• 1,2,2-Trimethyl-1-propanol
• 1-Methyl-2,2-dimethylpropanol
• 1-tert-Butylethanol
• 2,2-Dimethyl-3-butanol
• 2-Butanol, 3,3-dimethyl-
• 3,3-Dimethyl-2-Butanol (2,2-3)
• 3,3-Dimethylbutan-2-Ol
• 3,3-Dymethyl-2butanol
• <span class="text-smallcaps">DL</span>-3,3-Dimethylbutan-2-ol
• Dymethylbutanol
• NSC 939
• Pinacolyl alcohol
• tert-Butyl methyl carbinol

3,3-Dimethyl-2-butanol, 98+%

CAS: 464-07-3

3,3-Dimethyl-2-butanol was used in conversion of ribose- and glucose-binding proteins into receptors for pinacolyl methyl phosphonic acid. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the

Formula: C₆H₁₄O

Purezza: 98+%

Colore e forma: Colorless, Liquid

Peso molecolare: 102.18

Ref: 02-043725

Pinacolone Alcohol

CAS: 464-07-3

Formula: C₆H₁₄O

Peso molecolare: 102.18

Ref: 4Z-P-653

3,3-dimethyl-2-butanol-d13

CAS: 464-07-3

Formula: C₆HD₁₃O

Peso molecolare: 102.18

Ref: 4Z-B-123010

3,3-Dimethyl-2-butanol

Prodotto controllato

CAS: 464-07-3

Applications 3,3-Dimethyl-2-butanol is used as a reagent in the synthesis of 2,4-dicarboxy-pyrroles as selective non-competitive mGluR1 antagonists. 3,3-Dimethyl-2-butanol is also used in the preparation of dihydropyrrole derivatives containing N-sulfanyl, sulfinyl, and sulfonyl moieties which have insecticidal activity.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Ito, M., et al.: Bioorg. Med. Chem., 11, 489 (2003); Micheli, F., et al.: Bioorg. Med. Chem., 11, 171 (2003)

Formula: C₆H₁₄O

Colore e forma: Neat

Peso molecolare: 102.175

Ref: TR-D471480

3,3-Dimethyl-2-butanol-d13

Prodotto controllato

CAS: 464-07-3

Formula: C₆D₁₃HO

Colore e forma: Neat

Peso molecolare: 115.255

Ref: TR-D471484

Pinacolyl alcohol

Prodotto controllato

CAS: 464-07-3

Pinacolyl alcohol is an organic compound with molecular weight of 186.25. It is a colorless liquid that is soluble in water and ether. Pinacolyl alcohol can be prepared by reacting chloral hydrate with acetaldehyde in the presence of a base, such as potassium carbonate or sodium bicarbonate. The reaction mechanism was studied using kinetic energy (KIE) values to determine the reaction rate order and equilibrium constants for the forward and reverse reactions. Pinacolyl alcohol has also been studied as a chemical substance that interacts with hydrochloric acid, chloride ions, and water vapor to form chloroform, hydrochloric acid, and water vapor respectively. These chemical reactions are reversible due to the presence of water vapor in the system.
Pinacolyl alcohol has been shown to be effective against inflammation in Sprague-Dawley rats by inhibiting cyclooxygenase enzymes which produce prostaglandins from arachidonic acid. This

Purezza: Min. 95%

Ref: 3D-FP146058