Interesting facts
Interesting Facts about 3-(allyltrisulfanyl)prop-1-ene
3-(allyltrisulfanyl)prop-1-ene is a fascinating compound that showcases the intriguing chemistry of sulfanes and alkenes. Here are some interesting aspects worth noting:
- Structure and Reactivity: This compound features a trisulfanyl group, which consists of three sulfur atoms, attached to an allyl group. This unique arrangement of atoms enhances its reactivity, making it an interesting subject for study in organic synthesis.
- Thiomolecular Interaction: The presence of sulfur provides opportunities for intriguing interactions with various metals and other reagents, leading to potential applications in catalysis and material science.
- Biochemical Significance: Compounds with sulfur functionalities often play critical roles in biological systems. They can be involved in various biological processes such as enzyme catalysis and redox reactions.
- Applications in Organic Synthesis: Due to its reactive double bond and unique sulfur structure, 3-(allyltrisulfanyl)prop-1-ene has potential implications in organic synthesis, particularly in the development of thiol-based compounds.
- Sustainability Perspective: Sulfur-containing compounds are of increasing interest in sustainable chemistry due to their potential to replace more toxic substances in chemical reactions, showcasing a move towards greener chemistry.
In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." Exploring compounds like 3-(allyltrisulfanyl)prop-1-ene opens the door to numerous possibilities in research and application.
As you delve deeper into the world of chemistry, remember that every compound tells a story. The unique properties of 3-(allyltrisulfanyl)prop-1-ene may inspire new ideas and innovations in both academic and industrial settings.
Synonyms
Diallyl trisulfide
2050-87-5
ALLYL TRISULFIDE
Allitridin
Trisulfide, di-2-propenyl
Diallyltrisulfide
Diallyl trisulphide
allitridum
diallyltrisulfane
Di-2-propenyl trisulfide
Dasuansu
FEMA No. 3265
3-(prop-2-enyltrisulfanyl)prop-1-ene
CCRIS 3251
EINECS 218-107-8
0ZO1U5A3XX
NSC651936
NSC 651936
ALLITRIDE
BRN 1745734
bis(prop-2-en-1-yl)trisulfane
DTXSID9045972
CHEBI:78492
AI3-35127
NSC-651936
(CH2=CHCH2S)2S
DIALLYL TRISULFIDE [MI]
DTXCID7025972
DIALLYL TRISULFIDE [FHFI]
Trisulfide, di-2-propenyl (9CI)
0-01-00-00441 (Beilstein Handbook Reference)
DIALLYL TRISULFIDE [WHO-DD]
Di-2-propenyl Trisulfides
3-prop-2-enylsulfanyldisulfanylprop-1-ene
allitridi
Trisulfide, di-2-propen-1-yl
8008-99-9
Diprop-2-en-1-yltrisulfane
CHEMBL123040
Prop-2-enyl prop-2-enylthio disulfide
NCGC00095290-01
Diallyl Trisulfide (80%)
UNII-0ZO1U5A3XX
3-(allyltrisulfanyl)prop-1-ene
Di-allyl-trisulfide
1,3-Diallyltrisulfane
Allyl trisulfide, 8CI
Trisulfide di-2-propenyl
1,3-Diallyltrisulfane #
SCHEMBL562845
SPECTRUM1505014
FEMA 3265
4,5,6-Trithia-1,8-nonadiene
Diallyl Trisulfide (80per cent)
Tox21_111500
BDBM50318454
MSK001687
Diallyl trisulfide, >=97% (HPLC)
Diallyl trisulfide, >=98% (HPLC)
AKOS006282485
CCG-230978
FD41115
FG36532
NCGC00095290-02
AS-75640
CAS-2050-87-5
DB-003624
HY-117235
CS-0064491
NS00021054
Q17148332
Garlic extract Mixture of mainly diallyldisulfide and diallyl trisulfide
Solubility of 3-(allyltrisulfanyl)prop-1-ene
3-(allyltrisulfanyl)prop-1-ene presents unique solubility characteristics that are influenced by its molecular structure and functional groups. Understanding the solubility of this compound requires consideration of several factors:
In summary, while 3-(allyltrisulfanyl)prop-1-ene may exhibit limited solubility in aqueous environments, it is likely more soluble in organic solvents such as ether or chloroform. These characteristics make it an interesting compound for further exploration in chemical processes.