Interesting facts
Interesting Facts about 2-(2,2-dimethylpropanoyl)indane-1,3-dione
The compound 2-(2,2-dimethylpropanoyl)indane-1,3-dione is a fascinating member of the diketone family, showcasing the intriguing chemistry of indane derivatives. This compound possesses unique structural characteristics that contribute to its diverse reactivity and applications in various fields.
Key Highlights:
- Structural Complexity: With its indane core and diketone functionality, this compound exhibits a structure that can facilitate a variety of chemical reactions, making it a valuable intermediate in organic synthesis.
- Potential Applications: The ability of 2-(2,2-dimethylpropanoyl)indane-1,3-dione to act as a precursor opens up potential applications in pharmaceuticals, agrochemicals, and materials science.
- Reactivity: The presence of two carbonyl groups in its structure enhances the compound's reactivity, allowing for various nucleophilic additions, making it a useful building block for more complex molecules.
As a student or researcher, exploring the chemistry of this compound can offer insights into:
- Reaction mechanisms involving diketones and indane derivatives.
- The role of sterics and electronics in reactivity patterns.
- Potential modifications to enhance its pharmacological properties or functional applications.
In summary, 2-(2,2-dimethylpropanoyl)indane-1,3-dione is not just a chemical compound but a gateway to understanding intricate organic synthesis, paving the way for innovative research and development in multiple scientific domains.
Synonyms
PINDONE
83-26-1
Chemrat
Pivalyl
Pivalyn
Pival
2-Pivaloyl-1,3-indandione
2-Pivaloylindane-1,3-dione
Pivacin
Pindon
2-Pivalyl-1,3-indandione
Pivalyl Valone
Tri-Ban
Pivaldion
Pivaldione
1,3-Indandione, 2-pivaloyl-
NSC 31211
Caswell No. 671
Pindone [BSI:ISO]
1H-Indene-1,3(2H)-dione, 2-(2,2-dimethyl-1-oxopropyl)-
2-Pivaloyl-indan-1,3-dion
2-Pivaloyl-indaan-1,3-dion
Latka 333
CCRIS 4862
HSDB 1756
UNII-2KFI1XBH7G
2KFI1XBH7G
Pivalyl indan-1,3-dione
Pivalyl indandione
EINECS 201-462-8
2-Pivaloylindan-1,3-dione
2-(Trimetil-acetil)-indan-1,3-dione
EPA Pesticide Chemical Code 067703
BRN 2051258
DTXSID1025930
AI3-01946
2-(2,2-dimethylpropanoyl)indene-1,3-dione
PINDONE [HSDB]
PINDONE [ISO]
PINDONE [MI]
2-(Trimethylacetyl)-1,3-indandione
NSC-31211
2-(2,2-Dimethyl-1-oxopropyl)-1H-indene-1,3(2H)-dione
DTXCID205930
CHEBI:82261
1, 2-pivaloyl-
UN 2472
1, 2-pivalyl-
Paracakes
Contrax-P
Para-Pac
Pindon [Dutch]
Pivaldion [Italian]
Pivaldione [French]
2-(2,3-[2H]-dione
2-(2,2-dimethyl-1-oxopropyl)-1H-indene-1,3-(2H)-dione
Latka 333 [Czech]
2-Trimethylacetyl-1,3-indandione
tert-Butyl valone
CAS-83-26-1
WLN: L56 BV DV CHJ CVX1&1&1
1H-Indene-1, 2-(2,2-dimethyl-1-oxopropyl)-
2-(2,2-Dimethylpropanoyl)-1H-indene-1,3(2H)-dione
2-Pivaloyl-indaan-1,3-dion [Dutch]
2-Pivaloyl-indan-1,3-dion [German]
1,3-Dioxo-2-pivaloy-lindane
tertButyl valone
2-(Trimetil-acetil)-indan-1,3-dione [Italian]
Pindone 2-Pivalyl-1,3-indandione
Pival (OSHA)
2Pivalyl1,3indandione
1,3Dioxo2pivaloylindan
pivaloylindan-1,3-dione
Pindone (ACGIH:OSHA)
SCHEMBL435148
1,3-Indandione, 2-pivalyl-
PIVALYLINDAN-1,3-DIONE
CHEMBL1369243
NSC6281
NSC-6281
NSC31211
2-Pivalyl-1,3-indandione (OSHA)
Tox21_201353
Tox21_303317
AKOS028108439
USEPA/OPP Pesticide Code: 067703
NCGC00090859-01
NCGC00090859-02
NCGC00090859-03
NCGC00257075-01
NCGC00258905-01
FP169052
Pindone, PESTANAL(R), analytical standard
2,2-DIMETHYLPROPOXY-1,3-INDANDIONE
NS00007372
C19141
Q2276931
2-(2,2-Dimethylpropanoyl)-1H-indene-1,3(2H)-dione #
2-(2,2-Dimethyl-1-oxopropyl)-1H-indene-1,3 (2H)-dione
2,3-dihydro-2-(2,2-dimethyl-1-oxopropyl)-1H-indene-1,3-dione
201-462-8
Solubility of 2-(2,2-dimethylpropanoyl)indane-1,3-dione
The solubility of the compound 2-(2,2-dimethylpropanoyl)indane-1,3-dione can be influenced by various factors, including its molecular structure and the nature of the solvent. Generally, understanding solubility involves considering the following key aspects:
Many compounds in this class may have moderate to low solubility in water, which is consistent with the trend of many aromatic derivatives. As stated, "like dissolves like," indicating that polar solutes are better soluble in polar solvents while non-polar solutes favor non-polar solvents. Thus, for 2-(2,2-dimethylpropanoyl)indane-1,3-dione, it is advisable to test solubility in various organic solvents to identify the most suitable medium for applications.