634892-64-1 Usage
Molecular structure
Complex The molecular structure of 1H-Indole,4,5,6,7-tetrahydro-1-(1-methylethenyl)-(9CI) is complex, with multiple rings and chains.
Member of indole group
Yes 1H-Indole,4,5,6,7-tetrahydro-1-(1-methylethenyl)-(9CI) is a member of the indole group of chemicals.
Natural sources
Plants and fungi This chemical is commonly found in natural sources such as plants and fungi.
Biological activities
Diverse range 1H-Indole,4,5,6,7-tetrahydro-1-(1-methylethenyl)-(9CI) is known for its diverse range of biological activities.
Industrial applications
Synthesis of pharmaceuticals, agrochemicals, and fragrance compounds This chemical is used in various industrial applications, including the synthesis of pharmaceuticals, agrochemicals, and fragrance compounds.
Essential oil of Melaleuca armillaris leaves
Part of 1H-Indole,4,5,6,7-tetrahydro-1-(1-methylethenyl)-(9CI) is a part of the essential oil of Melaleuca armillaris leaves.
Antioxidant and antimicrobial properties
Exhibits This chemical has been found to exhibit antioxidant and antimicrobial properties.
Potential applications in treatment
Various diseases and disorders 1H-Indole,4,5,6,7-tetrahydro-1-(1-methylethenyl)-(9CI) has been studied for its potential applications in the treatment of various diseases and disorders.
Check Digit Verification of cas no
The CAS Registry Mumber 634892-64-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,4,8,9 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 634892-64:
(8*6)+(7*3)+(6*4)+(5*8)+(4*9)+(3*2)+(2*6)+(1*4)=191
191 % 10 = 1
So 634892-64-1 is a valid CAS Registry Number.
634892-64-1Relevant academic research and scientific papers
Comparison of the electronic and steric structures of 1-vinyl-and 1-(prop-1-en-1-yl)pyrroles according to the 1H and 13C NMR data
Afonin,Ushakov,Simonenko,Tarasova,Maksimova,Trofimov
, p. 397 - 405 (2007/10/03)
According to the 1H and 13C NMR data, 1-isopropenylpyrroles are characterized by larger dihedral angles between the heteroring and exocyclic double bond planes, as compared to isostructural 1-vinylpyrroles, due to steric effect of th
N-Isopropenylazoles: I. Direct N-Isopropenylation of Azoles with Propyne and Allene
Trofimov,Tarasova,Shemetova,Afonin,Klyba,Baikalova,Mikhaleva
, p. 408 - 414 (2007/10/03)
A number of previously unknown N-isopropenyl-substituted pyrroles, indoles, and di- and -triazoles were synthesized in 20-86% yield by reaction of the corresponding azole with an equilibrium mixture of propyne with allene or pure propyne and allene in the system KOH-DMSO (105-145°C, 5-15 h, atmospheric or elevated pressure). The reaction is regioselective. The electronic and steric structure and the degree of conjugation between the exocyclic double bond and the azole ring are discussed on the basis of the 1H and 13C NMR spectra. Almost complete absence of p-π conjugation in N-disubstituted N-isopropenylazoles have been found.
