Interesting facts
Interesting Facts about 2-ethylhexyl 2-sulfanylacetate
2-ethylhexyl 2-sulfanylacetate is a fascinating chemical compound that belongs to the family of thioesters. Its structure includes a sulfur atom, which provides unique properties to the compound. Here are some notable facts:
- Thioester Formation: The presence of the sulfur atom in thioesters like 2-ethylhexyl 2-sulfanylacetate significantly influences its reactivity compared to traditional esters. Generally, thioesters are more reactive, which can be advantageous in various chemical reactions.
- Applications: This compound finds utility in several industrial applications, including its potential use in the production of specialty chemicals and fragrances. Its pleasant odor makes it appealing in the flavor and fragrance industry.
- Biochemical Relevance: Thioesters can play critical roles in biochemical processes. For example, they can serve as intermediates in metabolic pathways, involved in the synthesis and breakdown of fatty acids and amino acids.
- Synthetic Versatility: The synthesis of 2-ethylhexyl 2-sulfanylacetate can be achieved through various synthetic routes, allowing chemists to tailor it for specific applications. This flexibility makes it a useful building block in organic synthesis.
- Environmental Impact: Understanding the behavior of thioesters in the environment is crucial since they may participate in metabolic and degradation pathways, affecting their environmental persistence and toxicity.
In conclusion, 2-ethylhexyl 2-sulfanylacetate exemplifies the intriguing chemistry surrounding thioesters. The compound’s unique structure and properties open avenues for further research and development in various fields, making it an exciting subject for chemists and industry professionals alike.
Synonyms
2-Ethylhexyl thioglycolate
7659-86-1
Thioglycolic acid 2-ethylhexyl ester
2-Ethylhexyl mercaptoacetate
ACETIC ACID, MERCAPTO-, 2-ETHYLHEXYL ESTER
Mercaptoacetic acid 2-ethylhexyl ester
2-Ethylhexylthioglycolate
2-EHTG
Thioglykolsaeure-2-aethylhexyl ester
EINECS 231-626-4
X6P51ASB6H
2-ethylhexyl 2-mercaptoacetate
DTXSID4027656
Thioglykolsaeure-2-aethylhexyl ester [German]
DTXCID807656
Acetic acid, 2-mercapto-, 2-ethylhexyl ester
EC 231-626-4
231-626-4
2-ethylhexyl 2-sulfanylacetate
32885-07-7
2-mercaptoacetic acid 2-ethylhexyl ester
CAS-7659-86-1
Thioglycolic Acid Octyl Ester
MFCD00022081
UNII-X6P51ASB6H
SCHEMBL27210
2-Ethylhexyl sulfanylacetate #
CHEMBL1869371
OWHSTLLOZWTNTQ-UHFFFAOYSA-
Tox21_201541
Tox21_303486
AKOS000120360
NCGC00164377-01
NCGC00164377-02
NCGC00257281-01
NCGC00259091-01
LS-13895
DB-021307
NS00004386
T0612
2-Ethylhexyl thioglycolate, >=95.0% (GC)
F71198
Q27887386
InChI=1/C10H20O2S/c1-3-5-6-9(4-2)7-12-10(11)8-13/h9,13H,3-8H2,1-2H3
Solubility of 2-Ethylhexyl 2-Sulfanylacetate
The solubility of 2-ethylhexyl 2-sulfanylacetate in various solvents can be influenced by several factors, including its molecular structure and the nature of the solvent. Here are some key points to consider:
Ultimately, while specific data on the solubility of 2-ethylhexyl 2-sulfanylacetate might be limited, its behavior in a range of solvents typically aligns with the trends observed in similar organic compounds.