22958-05-0 Usage
Derivative of indole
Heterocyclic organic compound This compound is derived from the base structure of indole, which is a heterocyclic (containing atoms of different elements) organic compound.
Chemical modification
4-nitrobenzoyl group The specific modification in this compound involves the addition of a 4-nitrobenzoyl group, which influences its properties and reactivity.
Yellowish appearance
Color 1H-Indole, 1-(4-nitrobenzoyl)has a yellowish color, which is a characteristic physical property.
Insoluble in water
Solubility This compound does not dissolve well in water, which is an important consideration for its applications and handling.
Soluble in organic solvents
Solubility 1H-Indole, 1-(4-nitrobenzoyl)dissolves in certain organic solvents, which is useful for its processing and use in chemical reactions.
Organic synthesis and chemical research
Application This compound is commonly used as a building block in the synthesis of various pharmaceuticals and biologically active compounds, making it valuable in the fields of organic synthesis and chemical research.
Building block for drug development
Role in drug development The structure and properties of 1H-Indole, 1-(4-nitrobenzoyl)make it suitable for use as a building block in the development of new drugs and chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 22958-05-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,5 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 22958-05:
(7*2)+(6*2)+(5*9)+(4*5)+(3*8)+(2*0)+(1*5)=120
120 % 10 = 0
So 22958-05-0 is a valid CAS Registry Number.
22958-05-0Relevant articles and documents
A novel one-pot synthesis of N-acylindoles from primary aromatic amides
Abid, Mohammed,De Paolis, Omar,T?r?k, Béla
, p. 410 - 412 (2008/09/17)
A novel one-pot synthesis of N-acylindoles via tandem cycloalkylation- annelation is described. This approach is based on the use of a strong solid-acid catalyst, montmorillonite K-10, and microwave irradiation under solvent-free conditions. The tandem cy
