Interesting facts
Interesting Facts about 2-(Chloromethyl)thiirane
2-(Chloromethyl)thiirane is a fascinating compound in the realm of organic chemistry, particularly known for its unique structural characteristics and reactive properties. Here are some intriguing points to note about this compound:
- Functional Group Diversity: The compound features a thiirane structure, which belongs to the family of cyclic sulfides. This ring structure is distinctive and contributes to its interesting chemical reactivity.
- Chloromethyl Group: The presence of a chloromethyl group introduces unique substituent properties, making it a valuable intermediate in organic synthesis.
- Synthesis Route: 2-(Chloromethyl)thiirane can be synthesized through various methods, including reactions involving sulfur compounds. Its formation often involves a careful consideration of ring strain and sterics due to the three-membered ring.
- Applications: This compound finds its applications as a building block in the synthesis of more complex organic molecules. It is particularly useful in the pharmaceutical and agrochemical industries.
- Reactivity: The presence of the chlorine atom makes it susceptible to nucleophilic substitution reactions, a vital characteristic that allows for diverse transformations in synthetic organic chemistry.
In summary, 2-(Chloromethyl)thiirane stands as an important compound in the study of sulfur-containing heterocycles. Its ability to undergo numerous chemical reactions while serving as a precursor for more complex entities highlights its significance in the field. As stated by renowned chemist, "the study of small molecules like this one often leads to great discoveries," underscoring the profound impact of seemingly simple compounds in advancing chemical science.
Synonyms
2-(Chloromethyl)thiirane
EPITHIOCHLOROHYDRIN
3221-15-6
Thioepichlorohydrin
3-Chloropropylene sulfide
(Chloromethyl)thiirane
Thioepichlorhydrin
Chloropropylene sulfide
2-Thiiranylmethyl chloride
Thiirane, (chloromethyl)-
1-Chloro-2,3-epithiopropane
Chloropropylene sulphide
Thiirane, 2-(chloromethyl)-
2-(Chloromethyl)ethylene sulfide
Propane, 1-chloro-2,3-epithio-
Thiirane, 2-chloromethyl-
3-Chloropropene sulfide
NSC 36644
BRN 0102466
5N825YLR9Q
3-Chloro-1,2-propylene sulfide
AI3-18238
NSC-36644
DTXSID701031297
5-17-01-00026 (Beilstein Handbook Reference)
DTXCID701516302
807-683-1
MFCD00041199
Epithiochlorhydrin
Epithiochlorhydrine
epithiochlorohydrine
UNII-5N825YLR9Q
2-(chloromethyl)-thiirane
WLN: T3STJ B1G
SCHEMBL572580
(2R)-2-(chloromethyl)thiirane
2298446-09-8
NSC36644
BBL103412
GEO-01283
STL557222
AKOS005254618
MS-20615
CS-0232950
EN300-129675
G74669
Q27262592
Solubility of 2-(chloromethyl)thiirane
2-(chloromethyl)thiirane, also known by its systematic name, is an intriguing compound with specific solubility characteristics. This compound is categorized based on its functional groups, which influence its interactions with solvents.
Solubility Characteristics
The solubility of 2-(chloromethyl)thiirane can be summarized with a few key points:
As stated, "Like dissolves like," indicating that the solubility is often enhanced when the solute and solvent possess similar polar characteristics. Therefore, for practical applications, understanding these solubility trends is essential in selecting appropriate solvents for reactions or extractions involving 2-(chloromethyl)thiirane.
In summary, the solubility profile of 2-(chloromethyl)thiirane reveals much about its chemical behavior and practical usability in various chemical processes.