Interesting facts
Interesting Facts about 2,2-Dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarbonyl Chloride
2,2-Dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarbonyl chloride is a fascinating compound that showcases the complexity and versatility of organic chemistry. Here are some intriguing facts about this compound:
- Structural Uniqueness: The compound features a cyclopropane ring, which is a three-membered carbon ring known for its angle strain and reactivity. This characteristic makes cyclopropanes interesting subjects in organic synthesis.
- Functional Groups: This compound contains not only a cyclopropane structure but also a carbonyl chloride functional group, known for its reactivity in nucleophilic acyl substitution reactions. This adds to the compound’s utility in synthetic organic chemistry.
- Synthetic Applications: The presence of multiple substituents and functional groups makes this compound a potential intermediate in the synthesis of more complex organic molecules, particularly in pharmaceutical applications.
- Reactivity: Given the presence of the carbonyl chloride, this compound is expected to react readily with nucleophiles, leading to the formation of various derivatives, such as amides and esters.
- Environmental Considerations: As a compound containing chlorine, careful handling and disposal are crucial due to potential environmental impacts. Understanding the chemical reactivity is essential for both safety and compliance with regulations.
In conclusion, 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarbonyl chloride not only embodies the intricacies of organic synthesis but also serves as a reminder of the responsibilities that come with working with reactive compounds. As stated by many chemists, "Every compound we explore has a story to tell, with implications for both nature and innovation."
Synonyms
EINECS 224-780-9
(1R-trans)-2,2-Dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarbonyl chloride
224-780-9
Chrysanthemoyl chloride
14297-81-5
Cyclopropanecarbonylchloride, 2,2-dimethyl-3-(2-methyl-1-propen-1-yl)-
2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carbonyl chloride
Chrysanthemic acid chloride
53955-46-7
Chrysanthemumoyl chloride
Chrysanthemumic acid chloride
Chrysanthemummonocarbonyl chloride
(1R-cis)-2,2-Dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarbonyl chloride
EINECS 238-229-5
Chrysanthemoylchloride
Chrysanthemoyl-chlorid
Cyclopropanecarbonyl chloride, 2,2-dimethyl-3-(2-methyl-1-propenyl)-
CYCLOPROPANECARBONYL CHLORIDE, 2,2-DIMETHYL-3-(2-METHYLPROPENYL)-
SCHEMBL554915
DTXSID50931698
EINECS 258-886-1
AKOS006277116
2,2-DIMETHYL-3-(2-METHYLPROP-1-EN-1-YL)CYCLOPROPANE-1-CARBONYL CHLORIDE
NS00087519
2,2-dimethyl-3-(1-isobutenyl)-cyclopropanecarboxylic acid chloride
2,2-Dimethyl-3-(2-methyl-1-propenyl)-cyclopropanecarbonylchloride
2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarbonyl chloride
2,2-dimethyl-3-isobutenylcyclopropane-1-carboxylic acid chloride
3-(2-methyl-1-propenyl)-2,2-dimethylcyclopropanecarboxylic chloride
3-(2-methyl-1-propenyl)-2,2-dimethylcyclo-propanecarboxylic acid chloride
3-(2-methyl-1-propenyl)-2,2-dimethylcyclopropanecarboxylic acid chloride
Solubility of 2,2-Dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarbonyl Chloride
The solubility of 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarbonyl chloride in various solvents can be quite intriguing. Due to its unique structural characteristics, the behavior of this compound in different media provides insights into its physicochemical properties. Below are some notable points regarding its solubility:
To summarize, the solubility of 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarbonyl chloride varies notably between polar and non-polar solvents, largely influenced by its chemical structure. As stated, "solubility is often a key determiner of a compound's chemical behavior," making this a crucial aspect in its study.