cas 142-30-3|| where to buy 2,5-Dimethyl-3-hexyne-2,5-diol

Nom du produit:2,5-Dimethyl-3-hexyne-2,5-diol

IUPAC Name:2,5-dimethylhex-3-yne-2,5-diol

: CAS：142-30-3; Formule moléculaire：C8H14O2; Pureté：98%

: Numéro de catalogue：CM116006; Poids moléculaire：142.2

Unité d'emballage	Stock disponible	Prix($)	Quantité
CM116006-500g	in stock	ŵȐ

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Détails du produit

: N° CAS:142-30-3; Formule moléculaire:C8H14O2; Point de fusion:-; Code SMILES:CC(O)(C)C#CC(O)(C)C; Densité:

: Numéro de catalogue:CM116006; Poids moléculaire:142.2; Point d'ébullition:121-123°C at 760 mmHg; N° Mdl:MFCD00004468; Stockage:Store at 2-8°C.

Category Infos

: Aliphatic Chain Compounds; Aliphatic chain compounds include aliphatic compounds and chain compounds containing other elements or groups. Aliphatic hydrocarbons are hydrocarbons with the basic properties of aliphatic compounds. In aliphatic compounds, carbon atoms are arranged in straight chain, branched chain or cyclic, which are respectively called straight chain aliphatic hydrocarbons, branched chain aliphatic hydrocarbons and alicyclic hydrocarbons. Some cyclic hydrocarbons are different in nature from aromatic hydrocarbons, and are very similar to aliphatic hydrocarbons. Such cyclic hydrocarbons are called alicyclic hydrocarbons. In this way, aliphatic hydrocarbons become a general term for all hydrocarbons except aromatic hydrocarbons. Aliphatic hydrocarbons and their derivatives (including halogenated hydrocarbons) and alicyclic hydrocarbons and their derivatives are collectively referred to as aliphatic compounds.

Column Infos

: Alcohols; Alcohol is a type of organic compound that carries at least one hydroxyl ( −OH) functional group bound to a saturated carbon atom.

Product Other Information

Product Overview	2,5-Dimethyl-3-hexyne-2,5-diol (2,5-DMHD) is a derivative of the cyclopentanone family of compounds that is used in a variety of scientific research applications. It is relatively non-toxic compound, which makes it an ideal choice for many experiments. 2,5-DMHD has demonstrated a wide range of biological activities, making it an attractive molecule for further research.
Physical Properties	It is a colorless and odorless compound.
Synthesis and Application	2,5-Dimethyl-3-hexyne-2,5-diol can be synthesized from the reaction of ethyl acetoacetate and 2-methyl-2-pentanol. This reaction is carried out in the presence of a base, such as sodium hydroxide, and a catalyst, such as p-toluenesulfonic acid. The reaction is typically carried out at a temperature of around 80°C. The reaction yields a crude product that can be purified by column chromatography. 2,5-Dimethyl-3-hexyne-2,5-diol has been used in a variety of scientific research applications. It has been used as a model compound to study the structure and reactivity of cyclopentanones. It has also been used to study the effects of substituents on the reactivity of cyclopentanones. Additionally, 2,5-Dimethyl-3-hexyne-2,5-diol has been used as a starting material in the synthesis of a variety of compounds, including bioactive molecules and polymers.
Future Directions	The potential future directions for 2,5-Dimethyl-3-hexyne-2,5-diol research are numerous. One potential direction is to further explore its antimicrobial properties. Additionally, its potential as an analgesic could be explored further. Finally, its potential to be used as a proton donor in various reactions could be further investigated.