Interesting facts
Interesting Facts about Benzylsulfanylmethylbenzene
Benzylsulfanylmethylbenzene, a fascinating organic compound, is a member of the thioether family, characterized by the presence of a sulfur atom bonded to two carbon-containing groups. This unique structure offers several intriguing aspects worth exploring:
- Versatile Applications: Due to its thioether linkage, benzylsulfanylmethylbenzene finds utility in a variety of applications such as organic synthesis and medicinal chemistry. Its functional groups can play crucial roles in the development of new pharmaceuticals.
- Flavor and Fragrance: Compounds with sulfur functionalities, like this one, are often explored in the fragrance industry. Their distinctive scents can enhance a product's appeal in cosmetics and perfumes.
- Biological Activity: Some thioethers, including benzylsulfanylmethylbenzene, have been studied for their biological activity. Researchers are investigating their potential in combating diseases, especially due to their anti-inflammatory properties.
- Interesting Synthesis: The synthesis of benzylsulfanylmethylbenzene can be achieved through various methods, including nucleophilic substitution reactions. This can provide an engaging laboratory exercise for chemistry students.
- Environmental Considerations: As with many organic compounds, understanding the environmental impact and degradation pathways of benzylsulfanylmethylbenzene is significant for chemical safety and sustainability efforts.
In summary, benzylsulfanylmethylbenzene not only showcases the beauty of organic chemistry but also highlights its importance in various industrial and medical applications. Its versatility continues to inspire research and development in multiple fields.
Synonyms
Dibenzyl sulfide
BENZYL SULFIDE
538-74-9
Benzyl thioether
Benzyl monosulfide
Dibenzyl monosulfide
Dibenzyl thioether
Sulfide, dibenzyl
1,3-Diphenyl-2-thiapropane
benzyl sulphide
Benzene, 1,1'-[thiobis(methylene)]bis-
1,1'-(Thiobis(methylene))bisbenzene
CCRIS 5969
NSC 212544
HSDB 2794
EINECS 208-703-6
Benzene, 1,1'-(thiobis(methylene))bis-
DTXSID6024599
AI3-00842
SULFIDE,DIBENZYL
1,1'-[thiobis(methylene)]dibenzene
NSC-212544
BENZYL SULFIDE [MI]
BENZYL SULFIDE [HSDB]
DTXCID704599
Q08048624M
1,1'-(thiobis(methylene))dibenzene
BENZENE, 1-1'-(THIOBIS(METHYLENE))BIS-
BENZENE, 1-1'-[THIOBIS(METHYLENE)]BIS-
Benzyl sulfide (8CI)
1,3Diphenyl2thiapropane
1,1'(Thiobis(methylene))bisbenzene
Benzene, 1,1'(thiobis(methylene))bis
inchi=1/c14h14s/c1-3-7-13(8-4-1)11-15-12-14-9-5-2-6-10-14/h1-10h,11-12h
dibenzylsulfane
Dibenzyl sulphide
benzylsulfanylmethylbenzene
dibenzylsulfide
[(Benzylsulfanyl)methyl]benzene
Benzene,1'-[thiobis(methylene)]bis-
MFCD00004784
Dibenzylsulfid
UNII-Q08048624M
Sulfide, dibenzyl-
SCHEMBL206
((Benzylthio)methyl)benzene
MLS002152894
(phenylmethylthio)methylbenzene
CHEMBL1369381
SCHEMBL11075647
(C6H5CH2)2S
NSC6648
(phenylmethylsulfanyl)methylbenzene
HMS2270O24
NSC-6648
Tox21_200326
NSC212544
STL482503
AKOS003626437
Dibenzyl sulfide, >=95.0% (HPLC)
1,1'-(sulfanediyldimethanediyl)dibenzene
NCGC00091191-01
NCGC00091191-02
NCGC00257880-01
AC-16469
CAS-538-74-9
SMR000112558
DB-052416
B0440
NS00042676
D88649
A829811
Q10374760
Solubility of Benzylsulfanylmethylbenzene
Benzylsulfanylmethylbenzene, a compound characterized by its unique structure, presents interesting solubility properties due to its chemical composition.
Generally, the solubility of a compound can be influenced by several factors:
In essence, “like dissolves like,” meaning that benzylsulfanylmethylbenzene is more likely to be soluble in nonpolar solvents (e.g., hexane or toluene) rather than in polar solvents. Therefore, one can expect:
When considering practical applications, it is important to remember that the solubility characteristics of benzylsulfanylmethylbenzene can affect its reactivity and behavior in a chemical environment.