Interesting facts
Interesting Facts about Isopropyl 2-[ethoxy-(isopropylamino)phosphinothioyl]oxybenzoate
The compound Isopropyl 2-[ethoxy-(isopropylamino)phosphinothioyl]oxybenzoate is indeed intriguing due to its multifaceted applications and unique structure. Here are some notable aspects:
- Versatile Applications: This compound is utilized in various fields such as agriculture, pharmaceuticals, and material science. Its derivatives often act as effective pesticides, showcasing its significance in agricultural practices.
- Phosphorus Chemistry: The presence of phosphorus in its structure allows it to participate in a variety of chemical reactions and forms a key part of biochemical processes, particularly those related to energy transfer and storage.
- Thioester Linkage: The thioyl group incorporated in the compound contributes to its reactivity and stability, making it an attractive candidate for synthesis applications.
- Amine Functionalization: The isopropylamino group enhances the compound's interaction with biological systems, potentially influencing its efficacy in target sites within living organisms.
- Safety Considerations: As with all chemical substances, understanding its safety profile is crucial. It must be handled with care, and proper safety protocols should always be followed during its use.
In the words of renowned chemist Linus Pauling, “The best way to have a good idea is to have a lot of ideas.” The exploration of compounds like isopropyl 2-[ethoxy-(isopropylamino)phosphinothioyl]oxybenzoate exemplifies this philosophy, where a diverse array of properties and potential applications sparks continuous research and innovation.
As the science of chemistry evolves, so does our understanding of complex compounds like this one. Each molecule opens new pathways for discovery and application, reinforcing the importance of ongoing study within the ethos of chemical research.
Synonyms
ISOFENPHOS
Isophenphos
25311-71-1
Oftanol
Amaze
Discus
Pyrfon
BAY-SRA-12869
DTXSID8032417
40 SD
BAY-92114
SRA 12869
SRA 128691
CHEBI:6009
0514MAW53A
O-Ethyl O-(2-isopropoxycarbonyl)phenyl isopropylphosphoramidothioate
1-Methylethyl-2-((ethoxy((1-methylethyl)amino)phosphinothioyl)oxy) benzoate
DTXCID6012417
Isopropyl salicylate O-ester with O-ethylisopropylphosphoramidothioate
2-((Ethoxy((1-methylethyl)amino)phosphinothioyl)oxy)benzoic acid 1-methylethyl ester
2-[[ethoxy[(1-methylethyl)amino]phosphinothioyl]oxy]benzoic acid 1-methylethyl ester
propan-2-yl 2-((ethoxy((propan-2-yl)amino)sulfanylidene-$l^(5)-phosphanyl)oxy)benzoate
propan-2-yl 2-({ethoxy[(propan-2-yl)amino]sulfanylidene-$l^{5}-phosphanyl}oxy)benzoate
RefChem:791864
246-814-1
LE-Mat
Isofenphos [BSI:ISO]
Amidocid
Pryfon
propan-2-yl 2-[ethoxy-(propan-2-ylamino)phosphinothioyl]oxybenzoate
Isopropylsalicylate, O-ester with O-ethyl isopropylphosphoramidothioate
Benzoic acid, 2-[[ethoxy[(1-methylethyl)amino]phosphinothioyl]oxy]-, 1-methylethyl ester
Caswell No. 447AB
isopropyl 2-((ethoxy(isopropylamino)phosphorothioyl)oxy)benzoate
Isophenphos [ISO-French]
Benzoic acid, 2-((ethoxy((1-methylethyl)amino)phosphinothioyl)oxy)-, 1-methylethyl ester
HSDB 6983
EINECS 246-814-1
103982-06-5
EPA Pesticide Chemical Code 109401
BRN 2949615
isopropyl 2-{[ethoxy(isopropylamino)phosphorothioyl]oxy}benzoate
UNII-0514MAW53A
AI3-27748
Isopropyl O-(ethoxy(isopropylamino)phosphinothioyl)salicylate
ISOFENPHOS [MI]
Isopropyl O-(ethoxy-N-isopropylamino(thiophosphoryl))salicylate
ISOFENPHOS [ISO]
Isopropyl salicylate ester of O-ethyl isopropylphosphoramidothioate
ISOFENPHOS [HSDB]
2-(O-Aethyl-N-isopropylamidothiophosphoryloxy)-benzosaeure-isopropylester [German]
Phosphoramidothioic acid, isopropyl-, O-ethyl O-(2-isopropoxycarbonylphenyl) ester
Salicylic acid, isopropyl ester, O-ester with O-ethyl isopropylphosphoramidothioate
SCHEMBL26546
Isofenphos, analytical standard
CHEMBL1882342
HOQADATXFBOEGG-UHFFFAOYSA-
MSK20063
Tox21_302219
Isopropyl salicylate O-ester with O-ethyl isopropylphosphoramidothioate
2-(O-Aethyl-N-isopropylamidothiophosphoryloxy)-benzosaeure-isopropylester
2-((Ethoxy((1-methylethyl)amino)phosphinothioyl)oxy) benzoic acid 1-methylethyl ester
Isofenphos 10 microg/mL in Cyclohexane
Isofenphos 100 microg/mL in Cyclohexane
NCGC00164274-01
NCGC00255226-01
103982-07-6
Benzoic acid, 2-((ethoxy((1-methylethyl)amino)phosphinothioyl)oxy)-, 1-methylethyl ester, (+)-
Benzoic acid, 2-((ethoxy((1-methylethyl)amino)phosphinothioyl)oxy)-, 1-methylethyl ester, (-)-
CAS-25311-71-1
NS00000159
Q15632850
Isopropyl 2-([ethoxy(isopropylamino)phosphorothioyl]oxy)benzoate #
O-Ethyl O-2-isopropoxycarbonylphenyl isopropylphosphoramidothioate
1-methylethyl 2-({ethoxy[(1-methylethyl)amino]phosphorothioyl}oxy)benzoate
propan-2-yl 2-({ethoxy[(propan-2-yl)amino]phosphorothioyl}oxy)benzoate
(RS)-(O-ETHYL O-2-ISOPROPOXYCARBONYLPHENYL ISOPROPYLPHOSPHORAMIDOTHIOATE)
1-METHYLETHYL 2-((ETHOXY((1-METHYLETHYL)AMINO)PHOSPHINOTHIOYL)OXY)BENZOATE
1-Methylethyl 2-[[ethoxy[(1-methylethyl)amino]phosphinothioyl]oxy]benzoate, 9CI
InChI=1/C15H24NO4PS/c1-6-18-21(22,16-11(2)3)20-14-10-8-7-9-13(14)15(17)19-12(4)5/h7-12H,6H2,1-5H3,(H,16,22)
Solubility of Isopropyl 2-[Ethoxy-(Isopropylamino)Phosphinothioyl]Oxybenzoate
The solubility of isopropyl 2-[ethoxy-(isopropylamino)phosphinothioyl]oxybenzoate in various solvents is an intriguing aspect of its chemical behavior. Understanding its solubility can help predict its behavior in different environments and its potential applications. Here are some key points to consider:
The interactions between the functional groups and the solvent molecules are crucial in determining the solubility of this compound. Understanding these interactions is not merely academic; it has practical implications in fields such as pharmaceuticals and chemical engineering.
As the saying goes, “Like dissolves like.” Therefore, it is essential to consider the chemical nature of both the solvent and the solute.
In summary, the solubility of isopropyl 2-[ethoxy-(isopropylamino)phosphinothioyl]oxybenzoate is influenced by:
These factors highlight the complexity of solubility and the importance of conditions in determining the fate of this compound in various environments.