74470-85-2 Usage
Uses
Used in Organic Synthesis:
2,3,3-Trimethyl-3H-benzo[g]indole is used as a key intermediate in organic synthesis for the production of various chemical compounds. Its unique structure and reactivity make it a valuable building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,3,3-Trimethyl-3H-benzo[g]indole is utilized as a starting material or a scaffold for the development of new drugs. Its versatile chemical properties and potential pharmacological activities, such as its role as an inhibitor of mitochondrial complex I, make it a promising candidate for drug discovery and design.
Used in Light-Emitting Devices:
2,3,3-Trimethyl-3H-benzo[g]indole is employed as a component in the development of light-emitting devices due to its photophysical properties. Its ability to emit light upon excitation makes it a suitable candidate for applications in optoelectronics and display technologies.
Used in Fluorescent Probes:
In the field of analytical chemistry, 2,3,3-Trimethyl-3H-benzo[g]indole is used as a fluorescent probe for the detection and analysis of various biomolecules and chemical species. Its fluorescence properties allow for sensitive and selective detection, making it a valuable tool in research and diagnostics.
Used in Antineoplastic Agents:
2,3,3-Trimethyl-3H-benzo[g]indole has been investigated for its potential use as an antineoplastic agent, demonstrating its ability to inhibit the growth of cancer cells. Its pharmacological activities make it a promising candidate for the development of novel cancer therapies and treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 74470-85-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,7 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74470-85:
(7*7)+(6*4)+(5*4)+(4*7)+(3*0)+(2*8)+(1*5)=142
142 % 10 = 2
So 74470-85-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H15N/c1-10-15(2,3)13-9-8-11-6-4-5-7-12(11)14(13)16-10/h4-9H,1-3H3
74470-85-2Relevant academic research and scientific papers
Ring transformations of heterocyclic compounds. XXII [1]. Pyrido[1,2-a]indolium salts from 2-methyl-3H-indoles by pyrylium mediated three carbon annelation
Zimmermann, Thomas,Hennig, Lothar
, p. 263 - 269 (2007/10/03)
The synthesis of pyrido[1,2-a]indolium perchlorates 8,11 from 2,4,6-triarylpyrylium perchlorates 1 and 2-methyl-3H-indoles 6,9 in the presence of a basic condensing agent (anhydrous sodium acetate, piperidine acetate, triethylamine/acetic acid, triethylamine) in ethanol by a 2,4-[C3+C2N] pyrylium ring transformation is reported. Spectroscopic data of the transformation products and their mode of formation are discussed.
Spiro-oxazine compound
-
, (2008/06/13)
A spiro-oxazine compound represented by the following general formula (A) or (A') is a photochromic compound having an excellent fatigue resistance to repetition of coloration and decoloration and an abundance of hues: STR1 wherein the α ring is a ring selected from a 5-membered ring having one N atom, which may be connected to a benzene ring or naphthalene ring, and a 6-membered ring having one N atom, with the proviso that the N atom in the αring is bonded to a C1-20 alkyl or another organic group, X is selected from O, S, Se and N--R1 (in which R1 is selected from H, and C1-20 alkyl and other organic groups), R2 and R3 are selected from --OH, amino, C1-20 alkoxy, halogen, and other groups, and k is an integer of 0 to 2.
