862135-61-3 Usage
Uses
Used in Pharmaceutical Development:
1H-Inden-2-ol, 5-bromo-2,3-dihydrois used as a key intermediate in the synthesis of new pharmaceutical compounds. Its unique structure and reactivity allow for the development of innovative drugs with potential therapeutic benefits.
Used in Agrochemicals:
In the agrochemical industry, 1H-Inden-2-ol, 5-bromo-2,3-dihydrois used as a precursor for the synthesis of bioactive molecules with pesticidal or herbicidal properties. Its unique chemical structure contributes to the development of effective and environmentally friendly agrochemicals.
Used in Organic Synthesis:
1H-Inden-2-ol, 5-bromo-2,3-dihydroserves as a versatile building block in the synthesis of various organic compounds. Its reactivity and unique functional groups make it a valuable component in the creation of novel molecules with diverse applications.
Used as a Reagent in Chemical Reactions:
Due to its unique properties, 1H-Inden-2-ol, 5-bromo-2,3-dihydrocan be employed as a reagent in various chemical reactions. Its ability to participate in a range of reactions, such as substitution, addition, or elimination, makes it a valuable tool in the synthesis of complex organic molecules.
Further research and testing are necessary to fully understand the potential uses and effects of 1H-Inden-2-ol, 5-bromo-2,3-dihydroin these industries, as well as to explore additional applications in other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 862135-61-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,1,3 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 862135-61:
(8*8)+(7*6)+(6*2)+(5*1)+(4*3)+(3*5)+(2*6)+(1*1)=163
163 % 10 = 3
So 862135-61-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H9BrO/c10-8-2-1-6-4-9(11)5-7(6)3-8/h1-3,9,11H,4-5H2
862135-61-3Relevant articles and documents
A kind of indan -5 - carboxamide ROR γ regulator and its use
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Paragraph 0096; 0097; 0098; 0099; 0100; 0101; 0102, (2019/03/15)
The invention relates to a structure of formula (I) compound of formula or a stereoisomer thereof, tautomers or its pharmaceutically acceptable salt or solvate or prodrug, its preparation method, a pharmaceutical composition containing these modulators and their use in the treatment ROR γ-mediated inflammatory, metabolic and autoimmune disorders.
Concise syntheses of 2-aminoindans via indan-2-ol
G?ksu, Süleyman,Se?en, Hasan
, p. 6801 - 6807 (2007/10/03)
2-Amino-5,6-dimethoxyindan hydrochloride was synthesized in seven steps and with an overall yield of 48%. Indan-2-ol was converted to 5,6-dibromo-indan-2- ol in three steps by acetylation, electrophilic bromination and deacetylation. Dimethoxylation of 5,6-dibromoindan-2-ol with NaOCH3 in the presence of CuI gave 5,6-dimethoxy-indan-2-ol, which was converted to 2-amino-5,6-dimethoxyindan hydrochloride by azidation, followed by Pd-C catalyzed hydrogenation. Similarly, 2-amino-5-bromoindan was synthesized in five steps and with an overall yield of 50%. Indan-2-ol was converted to 2-aminoindan by azidation followed by Pd-C catalyzed hydrogenation. The reaction of 2-aminoindan with 2.5 equiv Br2 afforded 2-amino-5,6- dibromoindan.
Use of oxirane ring-opening reactions for synthesis of ethylene- bis(indenyl) ligands containing alkene tethers
Panarello, Anthony P.,Vassylyev, Oleksiy,Khinast, Johannes G.
, p. 797 - 800 (2007/10/03)
An efficient strategy is presented for the synthesis of novel bis-indenyl ligands containing alkene tethers for their further immobilization. The tether was attached to a bridge or aromatic ring of the ligand. The ligands were prepared using oxirane ring-opening reaction.
