1082470-14-1 Usage
Molecular weight
203.24 g/mol The mass of one mole of the compound, based on its molecular formula.
Appearance
Off-white solid The physical appearance of the compound, typically as a crystalline solid.
Solubility
Slightly soluble in water, soluble in organic solvents The compound's ability to dissolve in different solvents, which is important for its applications in various industries.
Melding point
140-145°C The temperature range at which the compound transitions from a solid to a liquid state, which is useful for its purification and processing.
Derivation
Derived from indole The starting material from which the compound is synthesized, indicating its natural occurrence in plants and animals.
Building block in synthesis
Used in the production of pharmaceuticals, agrochemicals, and other organic compounds The compound's role as an intermediate in the synthesis of various products, highlighting its versatility.
Potential use in new materials
Studied for its possible applications in the development of new materials, indicating its importance in materials science.
Precursor in production of dyes and pigments
Acts as a starting material in the synthesis of dyes and pigments, further showcasing its diverse applications.
Importance in chemistry and materials science
The compound's significant role in these fields due to its properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1082470-14-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,8,2,4,7 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1082470-14:
(9*1)+(8*0)+(7*8)+(6*2)+(5*4)+(4*7)+(3*0)+(2*1)+(1*4)=131
131 % 10 = 1
So 1082470-14-1 is a valid CAS Registry Number.
1082470-14-1Relevant articles and documents
Synthesis of indoles by copper-catalyzed heteroannulation of o-aminophenylboronic acid pinacol esters with β-keto esters
Bunescu, Ala,Wang, Qian,Zhu, Jieping
, p. 3811 - 3814 (2012)
Copper-catalyzed coupling of o-aminophenylboronic acid pinacol esters with β-keto esters afforded, under mild base-free oxidative conditions, 2,3-disubstituted indoles featuring a key Chan-Lam-type carbon-carbon bond-forming reaction. Georg Thieme Verlag KG · Stuttgart · New York.
Exploring the oxidative cyclization of substituted N-aryl enamines: Pd-catalyzed formation of indoles from anilines
Neumann, Julia J.,Rakshit, Souvik,Droege, Thomas,Wuertz, Sebastian,Glorius, Frank
supporting information; experimental part, p. 7298 - 7303 (2011/08/21)
The direct Pd-catalyzed oxidative coupling of two C-H-bonds within N-aryl-enamines 1 allows the efficient formation of differently substituted indoles 2. In this cross-dehydrogenative coupling, many different functional groups are tolerated and the starting material N-aryl-enamines 1 can be easily prepared in one step from commercially available anilines. In addition, the whole sequence can also be run in a one-pot fashion. Optimization data, mechanistic insight, substrate scope, and applications are reported in this full paper. Copyright
