Product Name:2,5-Dimethyl-3-hexyne-2,5-diol

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

CAS:142-30-3
Molecular Formula:C8H14O2
Purity:98%
Catalog Number:CM116006
Molecular Weight:142.2

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CM116006-500g in stock ƻǧ

For R&D use only.

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Product Details

CAS NO:142-30-3
Molecular Formula:C8H14O2
Melting Point:-
Smiles Code:CC(O)(C)C#CC(O)(C)C
Density:
Catalog Number:CM116006
Molecular Weight:142.2
Boiling Point:121-123°C at 760 mmHg
MDL No:MFCD00004468
Storage: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.