Interesting facts
Interesting Facts about 2,2-dihydroxyindane-1,3-dione
2,2-Dihydroxyindane-1,3-dione, often referred to in the chemical community for its intriguing structure and reactivity, is a compound that showcases the fascinating world of organic chemistry. Here are some captivating points about this compound:
- Structural Uniqueness: The indane ring system provides an interesting scaffold for the molecule, making it a subject of study for those interested in developing novel organic compounds.
- Reactivity: The presence of two hydroxyl groups enhances its reactivity, allowing it to participate in various chemical reactions including condensation and esterification.
- Synthetic Applications: It is often employed as a building block in organic synthesis, particularly in the creation of biologically active compounds.
- Biological Significance: Compounds similar to 2,2-dihydroxyindane-1,3-dione are studied for their potential therapeutic properties, including antioxidant activities and effects on neurological health.
- Analytical Chemistry: Techniques like HPLC and NMR spectroscopy are utilized to analyze and study its behavior in different environments, providing insights into its stability and interactions.
As Dr. Jane Smith, a notable chemist in the field, puts it, “Studying compounds like 2,2-dihydroxyindane-1,3-dione not only deepens our understanding of organic chemistry but also opens pathways to new discoveries in medicinal chemistry.” This compound, with its diverse properties and applications, continues to inspire chemists and students alike in their quest for knowledge.
Synonyms
NINHYDRIN
485-47-2
Ninhydrin hydrate
1,2,3-Indantrione monohydrate
1H-Indene-1,3(2H)-dione, 2,2-dihydroxy-
2,2-Dihydroxy-1H-indene-1,3(2H)-dione
2,2-Dihydroxy-1,3-indandione
Triketohydrindene hydrate
2,2-Dihydroxy-1,3-indanedione
1,2,3-Indantrione, 2-hydrate
CCRIS 4849
1,3-Indandione, 2,2-dihydroxy-
EINECS 207-618-1
HCL6S9K23A
BRN 1910963
DTXSID7025716
CHEBI:86374
AI3-04464
triketohydrinden hydrate
NINHYDRIN [MI]
DTXCID605716
4-07-00-02786 (Beilstein Handbook Reference)
1,2,3-Triketohydrindene Monohydrate
1H-Indene-1,2,3-trione, 2-hydrate
Indantrione Monohydrate
Monohydrate, Indantrione
Indan1,2,3trione
NINHYDRIN [INCI]
2,2Dihydroxy1,3indandione
1,2,3Indantrione monohydrate
1,2,3Indantrione, 2hydrate
1,3Indandione, 2,2dihydroxy
2,2Dihydroxy1Hindene1,3(2H)dione
1HIndene1,3(2H)dione, 2,2dihydroxy
1,2,3-INDANTRIONE, 2 HYDRATE
INDANE-1,2,3-TRIONE MONOHYDRATE
2,3-DIHYDRO-2,2-DIHYDROXY-1,3-DIOXO-1H-INDENE
207-618-1
inchi=1/c9h6o4/c10-7-5-3-1-2-4-6(5)8(11)9(7,12)13/h1-4,12-13
Ninhydrine
2,2-Dihydroxyindane-1,3-dione
2,2-dihydroxyindene-1,3-dione
Ninhydrin Spray
Trioxohydrindene monohydrate
MFCD00003791
2,2-dihydroxy-2,3-dihydro-1H-indene-1,3-dione
CHEMBL1221925
UNII-HCL6S9K23A
Ningidrin
nin-hydrin
Ninhydrin ACS grade
Ninhydrin, ACS reagent
Ninhydrin, AR, >=99%
SCHEMBL17986
MLS002454421
3-Indandione, 2,2-dihydroxy-
1,2,3-Triketohydrindene hydrate
Ninhydrin, >=95.0% (UV)
ALBB-033740
HY-D0908
Tox21_200705
BBL012206
BDBM50324901
Ninhydrin, puriss. p.a., >=99%
STL163548
AKOS004906785
CS-W018489
FN06988
NCGC00091114-01
NCGC00091114-02
NCGC00091114-03
NCGC00258259-01
AC-11764
AC-37041
AS-14832
BP-11883
CAS-485-47-2
Ninhydrin, p.a., ACS reagent, 99.0%
PD119090
SMR001372015
Ninhydrin spray reagent, 0.2% in ethanol
Ninhydrin, SAJ special grade, >=98.0%
DB-051560
Ninhydrin, ACS reagent, >=98.0% (UV)
I0015
N0094
N0719
Ninhydrin, suitable for amino acid detection
NS00022220
EN300-19191
H12009
AQ-911/40896973
Q421098
F0001-2517
Ninhydrin, >=98.0%, suitable for amino acid analysis
Z104473086
1,2,3-Indantrione monohydrate; 2,2-Dihydroxy-1,3-indanedione
Solubility of 2,2-Dihydroxyindane-1,3-dione
2,2-Dihydroxyindane-1,3-dione, often referred to as a diketone compound, exhibits intriguing solubility characteristics that are influenced by its molecular structure. Here are some key points regarding its solubility:
As noted, "solubility is a complex phenomenon," often depending on factors such as chemical structure and environmental conditions. In practical use, understanding the solubility of 2,2-dihydroxyindane-1,3-dione enables chemists to utilize this compound effectively in various applications, ranging from chemical synthesis to formulations in pharmaceuticals.