94054-40-7 Usage
Chemical class
Pyrrole derivatives
Explanation
1-(4-methylbenzyl)-1H-pyrrole belongs to the class of pyrrole derivatives, which are aromatic heterocyclic compounds.
Explanation
At room temperature, this chemical compound appears as a yellow or brown colored solid.
Explanation
It is commonly used as an intermediate in the synthesis of pharmaceuticals and organic compounds.
Explanation
1-(4-methylbenzyl)-1H-pyrrole is known for its characteristic odor.
Explanation
It is often used in the production of insecticides and pesticides due to its chemical properties.
Explanation
Studies have shown that 1-(4-methylbenzyl)-1H-pyrrole has potential antibacterial and antifungal properties, making it valuable in the development of new medications and treatments.
Explanation
Due to its unique chemical properties, 1-(4-methylbenzyl)-1H-pyrrole serves various industrial and pharmaceutical applications.
Color
Yellow or brown
Usage
Intermediate in synthesis
Odor
Characteristic
Application
Insecticides and pesticides
Potential properties
Antibacterial and antifungal
Industrial and pharmaceutical applications
Various
Check Digit Verification of cas no
The CAS Registry Mumber 94054-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,0,5 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 94054-40:
(7*9)+(6*4)+(5*0)+(4*5)+(3*4)+(2*4)+(1*0)=127
127 % 10 = 7
So 94054-40-7 is a valid CAS Registry Number.
94054-40-7Relevant academic research and scientific papers
Decarboxylative formation of N-alkyl pyrroles from 4-hydroxyproline
Deb, Indubhusan,Coiro, Daniel J.,Seidel, Daniel
scheme or table, p. 6473 - 6475 (2011/06/28)
N-Alkyl pyrroles are obtained in a single step from 4-hydroxyproline and aldehydes in just 15 min under microwave irradiation.
Synthesis and nuclear magnetic resonance spectroscopic studies of 1- arylpyrroles
Lee, Chang Kiu,Jun, Jung Ho,Yu, Ji Sook
, p. 15 - 24 (2007/10/03)
A series of m- and p-substituted 1-phenyl, 1-benzyl, 1-benzoyl, and 1- (2-phenylethyl)pyrroles was prepared and their 1H and 13C nmr spectroscopic characteristics were examined. In general, good correlations were observed between the chemical shift values of the β-H and the β-C of pyrroles [except 1-(2-phenylethyl)pyrroles] and the Hammettt σ. The observation may be explained in terms of the electronic effects of the substituents which are transmitted through bonds and through space by interaction of the p orbitals between β-Cs of the pyrrole ring and m- and p- Cs of the phenyl ring. Substituent constants of 1-pyrrolyl, 1-pyrrolylmethyl, and 1-pyrroloyl groups for the 1H and 13C chemical shifts of phenyl ring are also presented.
