Interesting facts
Interesting Facts about 2-(Trichloromethylsulfanyl)isoindoline-1,3-dione
2-(Trichloromethylsulfanyl)isoindoline-1,3-dione is a fascinating compound known for its unique structural characteristics and potential applications in various fields. Here are some compelling aspects of this compound:
- Structural Insight: This compound belongs to the isoindoline family, which is notable for its bicyclic structure that consists of a six-membered ring fused to a five-membered ring. The presence of a trichloromethylsulfanyl group contributes to its intriguing chemical reactivity.
- Reactivity Profile: The trichloromethyl group is a powerful electrophile. Compounds containing this moiety are often studied for their ability to participate in nucleophilic substitution reactions, making them valuable intermediates in synthetic organic chemistry.
- Biological Significance: Like many compounds derived from isoindoline, derivatives may exhibit biological activity. Research into similar structures has shown potential in medicinal chemistry, particularly for developing new pharmaceuticals.
- Environmental Factors: The trichloromethyl group also raises concerns regarding environmental impact; compounds containing chlorine atoms can be persistent pollutants. Understanding the degradation pathways of such compounds is essential for environmental safety.
- Synthetic Utility: The synthetic versatility of 2-(trichloromethylsulfanyl)isoindoline-1,3-dione allows for the exploration of various chemical transformations, offering pathways to novel materials and compounds with desirable properties.
As a compound rich in both chemical reactivity and potential applications, 2-(trichloromethylsulfanyl)isoindoline-1,3-dione serves as an exciting subject for both research and development in the fields of chemistry and related sciences. Its unique nature holds promise for future discovery!
Synonyms
Folpet
133-07-3
Faltan
Orthophaltan
Phthaltan
Folpel
Spolacid
Folnit
Folpan
Ftalan
Intercide TMP
Acryptan
PHALTAN
Vinicoll
Fungitrol 11
Fungitrol
Phaltane
Faltex
Cosan I
N-(Trichloromethylthio)phthalimide
Thiophal
Trifol
Fungitrol II
Cosan T
1H-Isoindole-1,3(2H)-dione, 2-[(trichloromethyl)thio]-
Acryptane
Sanfol
2-(Trichloromethylsulfanyl)isoindole-1,3-dione
Dipet
Ortho phaltan 50W
Orthofaltan 50
Trichloromethylthiophthalimide
Folpel [French]
Murphy's rose fungicide
2-[(Trichloromethyl)thio]-1H-isoindole-1,3(2H)-dione
Folpex
Troysan anti-mildew O
N-(Trichloromethylmercapto)phthalimide
N-(Trichlormethylthio)phthalimide
N-(Trichloromethanesulphenyl)phthalimide
Folpet [ANSI:BSI:ISO]
N-(Trichlor-methylthio)-phthalamid
N-[(Trichloromethyl)thio]phthalimide
Phalton
ENT 26539
2-((Trichloromethyl)thio)-1H-isoindole-1,3(2H)-dione
Trichlormethylthioimid kyseliny ftalove
Trichloromethyl(thio)phthalimide
DTXSID0021385
CHEBI:82019
N-(Trichlor-methylthio)-phthalamid [German]
X5NFK36917
FOLPET [HSDB]
FOLPET [ISO]
Trichlormethylthioimid kyseliny ftalove [Czech]
FOLPET [MI]
N-(TRICHLOROMETHYL)THIOPHTHALIMIDE
1H-Isoindole-1,3(2H)-dione, 2-((trichloromethyl)thio)-
DTXCID101385
Folpet 100 microg/mL in Acetone
PHTHALIC ACID,IMIDE,N-TRICHLOROMETHYL SULFENYL
Folpet 100 microg/mL in Cyclohexane
N-((Trichloromethyl)thio)-Phthalimide
N-(trichloromethanesulfenyl)phthalimide
N-[(Trichloromethyl)thio]-Phthalimide
Phthalimide, N-((trichloromethyl)thio)-
Phthalimide, N-[(trichloromethyl)thio]-
2-[(Trichloromethyl)sulfanyl]-1H-isoindole-1,3(2H)-dione
Caswell No. 464
2-[(Trichloromethyl)thio]-1H-isoindole-1,3(2H)-dione, 9CI
2-[(trichloromethyl)sulfanyl]-2,3-dihydro-1H-isoindole-1,3-dione
N-((Trichloromethyl)thio)phthalimide
CAS-133-07-3
CCRIS 1036
HSDB 2651
EINECS 205-088-6
2-((Trichloromethyl)thio)isoindoline-1,3-dione
2-{(Trichloromethyl)thio}-1H-isoindole-1,3(2H)-dione
EPA Pesticide Chemical Code 081601
BRN 0193373
2-((Trichloromethyl)sulfanyl)-1H-isoindole-1,3(2H)-dione
2-((Trichloromethyl)thio)-1H-isoindole-1,3(2H)-dione, 9CI
UNII-X5NFK36917
2-((trichloromethyl)sulfanyl)-2,3-dihydro-1H-isoindole-1,3-dione
AI3-26539
Orthophaltan 50
Faltan (Standard)
Folpet (fungicide)
MFCD00047303
Troysan antimildew O
SCHEMBL19853
5-21-11-00118 (Beilstein Handbook Reference)
Ryl
N(Trichlormethylthio)phthalamid
N(Trichlormethylthio)phthalimide
CHEMBL1883819
N(Trichloromethylthio)phthalimide
HY-B1878R
Folpet 1000 microg/mL in Acetone
HY-B1878
Folpet 10 microg/mL in Cyclohexane
Tox21_201987
Tox21_301077
AC-997
AKOS015895774
N(Trichloromethanesulphenyl)phthalimide
Phthalimide, N((trichloromethyl)thio)
FF23542
USEPA/OPP Pesticide Code: 081601
NCGC00168313-01
NCGC00168313-02
NCGC00168313-03
NCGC00254978-01
NCGC00259536-01
AS-80226
Folpet, PESTANAL(R), analytical standard
2-(trichloromethylthio)isoindole-1,3-dione
CS-0013944
NS00005935
C18860
D95854
2((Trichloromethyl)thio)1Hisoindole1,3(2H)dione
A806547
Q426485
1HIsoindole1,3(2H)dione, 2((trichloromethyl)thio)
2-[(Trichloromethyl)sulfanyl]-1H-isoindole-1,3(2H)-dione #
205-088-6
Solubility of 2-(Trichloromethylsulfanyl)isoindoline-1,3-dione
The solubility characteristics of 2-(trichloromethylsulfanyl)isoindoline-1,3-dione are intricate, reflecting the compound's unique structure. Understanding its solubility involves considering several factors:
In summary, while specific solubility data may vary, the general expectation is that 2-(trichloromethylsulfanyl)isoindoline-1,3-dione has limited solubility in water but is better dissolved in organic solvents. Understanding these solubility properties is essential for applications where dissolution behavior is critical.