61861-90-3 Usage
Molecular Weight
173.19 g/mol
Structure
Bicyclic heterocycle with a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole, with a methyl group at the 3-position and a nitro group at the 7-position.
Polarity
Nonpolar (due to the balance of the charges in the molecule)
Solubility
Insoluble in water, soluble in organic solvents such as ethanol, methanol, and chloroform.
Reactivity
The presence of the nitro group makes the compound a potential precursor for the synthesis of various aromatic compounds. The methyl group adds to its chemical diversity and reactivity.
Applications
Potential applications in the synthesis of various organic compounds, drug development, and medicinal chemistry research due to the indole core structure commonly found in natural products and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 61861-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,6 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61861-90:
(7*6)+(6*1)+(5*8)+(4*6)+(3*1)+(2*9)+(1*0)=133
133 % 10 = 3
So 61861-90-3 is a valid CAS Registry Number.
61861-90-3Relevant articles and documents
One-pot N-alkylation/Heck approach to substituted indoles
Weinrich, Melissa L.,Beck, Hilary P.
experimental part, p. 6968 - 6972 (2010/02/27)
Here, we report the palladium-catalyzed one-pot N-alkylation/Heck cyclization of anilines to substituted indoles employing Pd(OAc)2/XPhos. The scope and limitations of this methodology will be described.
