113379-85-4 Usage
Molecular structure
1H-Pyrrole-3-carboxylic acid, 5-acetyl-1-methyl-2-phenyl-, ethyl ester has a complex molecular structure that includes a pyrrole ring, an acetyl group, a methyl group, a phenyl group, and an ethyl ester group.
Ester derivative
It is an ester derivative of 1H-pyrrole-3-carboxylic acid, 5-acetyl-1-methyl-2-phenyl, with an ethyl group attached to the carboxylic acid group.
Usage in organic synthesis and pharmaceutical research
Due to its potential biological and pharmacological activities, 1H-Pyrrole-3-carboxylic acid, 5-acetyl-1-methyl-2-phenyl-, ethyl ester is commonly used in organic synthesis and pharmaceutical research.
Potential in drug development
It shows promise in the development of new drugs and other important applications in the field of chemistry and medicine.
Specific properties
The specific properties of 1H-Pyrrole-3-carboxylic acid, 5-acetyl-1-methyl-2-phenyl-, ethyl ester are still being studied, but it is known to have potential biological and pharmacological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 113379-85-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,3,7 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 113379-85:
(8*1)+(7*1)+(6*3)+(5*3)+(4*7)+(3*9)+(2*8)+(1*5)=124
124 % 10 = 4
So 113379-85-4 is a valid CAS Registry Number.
113379-85-4Relevant academic research and scientific papers
Nucleophilic Addition to Oxazolium Salts: Stabilized Azomethine Ylides via 2-Substituted 4-Oxazolines
Vedejs, E.,Grissom, J.W.
, p. 1876 - 1882 (2007/10/02)
Treatment of oxazolium salts with cyanide generates 4-oxazolines 2 in situ.Ring opening to azomethine ylides 3 occurs spontaneously and 2 + 3 cycloadducts are obtained in the presence of acrylate, propiolate, or acetylenedicarboxylate dipolarophiles.In the case of acetylenic dipolarophiles, loss of HCN occurs under the reaction conditions and leads directly to pyrroles 5.The propiolate experiments are complicated by the formation of six-membered adducts 17 in some cases.This reaction pathway is explained by the addition of the acetylide anion derived from propiolate to the dipole, followed by cyclization.Sulfide nucleophiles can also be used to generate 4-oxazolines, but the yields of cycloadducts are lower.
