Indanes
Indanes are a class of cyclic hydrocarbons derived from benzene through the opening and subsequent reclosure of its ring, resulting in a five-membered ring structure. Indane, specifically, is characterized by the presence of an ethyl group attached to a five-membered ring containing three carbon atoms in a saturated or unsaturated form. This aromatic compound possesses unique physical and chemical properties due to its ring structure.
Indanes are widely used as intermediates in organic synthesis for the production of various chemicals such as dyes, pharmaceuticals, and agrochemicals. Their ability to undergo multiple types of reactions, including aromatization, alkylation, and cyclization, makes them valuable in industrial applications. Additionally, due to their structural flexibility, indanes can be derivatized into a wide range of functional groups, enhancing their utility in chemical processes.
The stability of the five-membered ring structure and its electron-donating properties contribute significantly to the reactivity and versatility of these compounds. Indanes are known for their high boiling points and low volatility, which are advantageous during manufacturing processes.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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2,3-dihydro-1H-indene-2-carbaldehyde | 37414-44-1 | C10H10O |
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2-(2,3-dihydro-1H-inden-1-yl)ethan-1-ol | 38425-66-0 | C11H14O |
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2-(5-Bromo-7-methyl-2,3-dihydro-1H-inden-4-yl)oxyacetohydrazide | 303010-22-2 | C12H15BrN2O2 |
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6H-Indeno[4,5-b]thiophene-4-carbonitrile,7,8-dihydro- | 313948-67-3 | C12H9NS |
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5-Bromo-2,3-dihydro-1H-inden-2-amine Hydrobromide | 321352-52-7 | C9H11Br2N |
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1H-Inden-1-ol,2,3-dihydro-3,3-dimethyl- | 38393-92-9 | C11H14O |
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Aprindine Hydrochloride | 33237-74-0 | C22H31ClN2 |
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N-(2,3-dihydroinden-1-ylidene)hydroxylamine | 3349-60-8 | C9H9NO |
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1H-Indene, 2,3-dihydro-1,2-dimethyl-, trans- | 70282-84-7 | C11H14 |
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1H-Indene, 1,1,2,2-tetrafluoro-2,3-dihydro- | 80829-35-2 | C9H6F4 |
Related Literature
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David White,Sean R. Stowell Biomater. Sci., 2017,5, 463-474
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Yong Ping Huang,Tao Tao,Zheng Chen,Wei Han,Ying Wu,Chunjiang Kuang,Shaoxiong Zhou,Ying Chen J. Mater. Chem. A, 2014,2, 18831-18837
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Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
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Brindha J.,Balamurali M. M.,Kaushik Chanda RSC Adv., 2019,9, 34720-34734
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