114747-48-7 Usage
Description
Spiro[2H-indole-2,3'-[3H]naphth[2,1-b][1,4]oxazine], 1,3-dihydro-1,3,3-triMethyl-6'-(4-Morpholinyl)is a heterocyclic organic compound characterized by its unique spiro-structure, which includes an indole and naphthoxazine ring system. Spiro[2H-indole-2,3'-[3H]naphth[2,1-b][1,4]oxazine], 1,3-dihydro-1,3,3-triMethyl-6'-(4-Morpholinyl)also features a 1,3-dihydro-1,3,3-triMethyl-6'-(4-Morpholinyl)group, which may contribute to its potential biological activities and applications in pharmaceutical and research fields. Its complex structure and properties make it an intriguing candidate for drug discovery and development, as well as for study in organic chemistry.
Uses
Used in Pharmaceutical Applications:
Spiro[2H-indole-2,3'-[3H]naphth[2,1-b][1,4]oxazine], 1,3-dihydro-1,3,3-triMethyl-6'-(4-Morpholinyl)is used as a potential therapeutic agent in the pharmaceutical industry due to its unique structure and possible biological activities. Its heterocyclic nature and spiro-configuration may offer advantages in the development of new drugs with novel mechanisms of action.
Used in Research Applications:
In the research field, Spiro[2H-indole-2,3'-[3H]naphth[2,1-b][1,4]oxazine], 1,3-dihydro-1,3,3-triMethyl-6'-(4-Morpholinyl)is used for studying the properties and behavior of heterocyclic organic compounds. Its complex structure makes it an interesting subject for investigations into organic chemistry, potentially leading to new insights and discoveries in the field.
Used in Drug Discovery and Development:
Spiro[2H-indole-2,3'-[3H]naphth[2,1-b][1,4]oxazine], 1,3-dihydro-1,3,3-triMethyl-6'-(4-Morpholinyl)is utilized in drug discovery and development processes to explore its potential as a new therapeutic agent. Its unique features may contribute to the creation of innovative drugs with improved efficacy and selectivity for various medical conditions.
Used in Organic Chemistry Studies:
In the field of organic chemistry, Spiro[2H-indole-2,3'-[3H]naphth[2,1-b][1,4]oxazine], 1,3-dihydro-1,3,3-triMethyl-6'-(4-Morpholinyl)is used for studying the synthesis, reactions, and properties of spiro-compounds. Its intricate structure provides a valuable opportunity to explore the chemistry of complex organic molecules and may lead to advancements in synthetic methods and understanding of molecular behavior.
Check Digit Verification of cas no
The CAS Registry Mumber 114747-48-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,7,4 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 114747-48:
(8*1)+(7*1)+(6*4)+(5*7)+(4*4)+(3*7)+(2*4)+(1*8)=127
127 % 10 = 7
So 114747-48-7 is a valid CAS Registry Number.
114747-48-7Relevant articles and documents
Microwave-Assisted Solvent-Free Synthesis of the Substituted Spiroindolinonaphth[2,1-b][1,4]oxazines
Koshkin,Fedorova,Lokshin,Guglielmetti,Hamelin,Texier-Boullet,Gromov
, p. 315 - 322 (2004)
The synthesis of the substituted spiroindolinonaphth[2,1-b][1,4]oxazines 3a-e is developed through the condensation of 2-methylene-1,3,3-trimethylindoline derivatives and 1-nitroso-2-naphthol under microwave irradiation. In the same conditions, in presence of morpholine the 6′-morpholinosubstituted compounds 4a, b, d, e are formed. The main advantages of the method are the short reaction time, solvent-free reaction condition, cleaner reaction products and the higher product yields in comparison with known methods of synthesis.
Synthesis, characterization and photochromic studies in film of heterocycle-containing spirooxazines
Tan, Ting-Feng,Chen, Pei-Li,Huang, Hua-Ming,Meng, Ji-Ben
, p. 8192 - 8198 (2007/10/03)
A series of novel heterocycle-containing spirooxazines have been designed and synthesized, and their photochromic properties were investigated under flash photolysis and continuous irradiation in particular regard to the fatigue resistance, the lifetime of the colored merocyanine form in various solutions and polymers. Especially, the characteristics of two UV-sensitive spirooxazines dispersed polymethylmethacrylate thin-films were extensively studied. Detailed studies showed that general significant shifts in the λmax of the absorption spectra of the open forms, interesting fatigue resistances and emission fluorescene properties were observed.
Protolysis of spironaphtho(aza)pyranoindoles
Gabbutt, Christopher D.,Hepworth, John D.,Heron, B. Mark,Partington, Steven M.
, p. 647/323 - 652/328 (2007/10/03)
Some novel amino-substituted spiroindolinonaphthopyrans have been synthesised. Whilst these compounds exhibit no observable photochromic properties at ambient temperature, protonation results in ring opening to given stable, intensely coloured dyes. Recyclisation and decolouration result on basification.
