Interesting facts
Interesting Facts about Methyl 2-Sulfanylacetate
Methyl 2-sulfanylacetate is a fascinating compound with a range of intriguing properties and applications. Here are some noteworthy facts:
- Source of Sulfur: This compound contains a thiol group, which is rich in sulfur. Sulfur-containing compounds often have distinctive odors, reminiscent of garlic or onion!
- Natural Occurrence: Methyl 2-sulfanylacetate can be found in various natural sources, particularly in certain plants and foods. It plays roles in flavor and aroma, making it interesting for the food industry.
- Reactivity: The presence of both methyl and thiol groups gives this compound unique reactivity. It can participate in diverse chemical reactions, such as nucleophilic substitutions and acylation processes, making it valuable in synthetic chemistry.
- Odor and Flavor: Due to its sulfur content, the compound can contribute to characteristic odors in certain foods, providing a unique sensory experience. This makes it a subject of interest for flavor chemists.
- Analytical Uses: Methyl 2-sulfanylacetate has applications in analytical chemistry, where it can be used as a marker or reactant in various analytical methods.
In summary, methyl 2-sulfanylacetate is not just a simple ester; it is a compound that bridges natural products and synthetic applications. The chemistry involved in understanding its properties showcases the intriguing intersection of organic chemistry and sensory science.
Synonyms
METHYL THIOGLYCOLATE
2365-48-2
Methyl mercaptoacetate
Methyl 2-mercaptoacetate
Thioglycolic acid methyl ester
Methylthioglycolate
Acetic acid, mercapto-, methyl ester
Acetic acid, 2-mercapto-, methyl ester
Methanethiol, methoxy-
Methylmercaptoacetate
USAF EK-7119
Mercaptoacetic acid methyl ester
Thioglykolsaeure-methylester
NSC 75117
HSDB 2705
2-mercaptoacetic acid methyl ester
EINECS 219-121-7
Thioglykolsaeure-methylester [German]
Methyl .alpha.-mercaptoacetate
BRN 0506259
O1608LA9EL
DTXSID0033673
NSC-75117
DTXCID8013673
METHYL THIOGLYCOLATE [MI]
EC 219-121-7
METHYL THIOGLYCOLATE [HSDB]
4-03-00-00614 (Beilstein Handbook Reference)
Methyl 2mercaptoacetate
Thioglykolsaeuremethylester
Methyl alpha-mercaptoacetate
METHYL THIOGLYCOLATE [INCI]
Acetic acid, mercapto, methyl ester
219-121-7
methyl 2-sulfanylacetate
Methyl sulfanylacetate
MFCD00004873
mercapto-acetic acid methyl ester
UNII-O1608LA9EL
methylthioglycolic ester
methyl-2-mercaptoacetate
Methyl sulfanylacetate #
thioglycolate methyl ester
Methyl 2-mercapto-acetate
methyl 2-sulfanylethanoate
Methyl thioglycolate, 95%
WLN: SH1VO1
SCHEMBL38833
mercapto-acetic acid methylester
CHEMBL1341329
MKIJJIMOAABWGF-UHFFFAOYSA-
Methyl ester of thioglycolic acid
NSC75117
Tox21_201130
BBL011360
STL146452
AKOS000120592
FM36432
NCGC00090993-01
NCGC00090993-02
NCGC00258682-01
BP-13329
CAS-2365-48-2
NS00001979
T1287
EN300-21066
E78832
A816826
Q27285190
F0001-0817
InChI=1/C3H6O2S/c1-5-3(4)2-6/h6H,2H2,1H3
ethyl 2-(tert-butyloxycarbonylamino)-2-pentafluorophenylacetate
Mercaptoacetic acid methyl ester;Thioglycolic acid methyl ester
Solubility of Methyl 2-Sulfanylacetate
Methyl 2-sulfanylacetate, often represented by its chemical formula C4H8O2S, exhibits interesting solubility characteristics that are largely influenced by its molecular structure. This compound is generally considered to be:
In general, the solubility of methyl 2-sulfanylacetate can be summarized as:
In practice, understanding the solubility of methyl 2-sulfanylacetate is crucial for researchers and chemists working on synthesis and formulation, as the solubility affects how the compound can be used in various applications.