130016-69-2 Usage
Methyl ester derivative
The compound is derived from alpha-methyl-1H-pyrrole-1-acetic acid by replacing the carboxylic acid group (-COOH) with a methyl ester group (-COOCH3).
Substituted pyrrole derivative
The compound is a derivative of pyrrole, which is a five-membered heterocyclic aromatic compound containing one nitrogen atom, with an additional alpha-methyl group (-CH3) attached to the ring.
Physical appearance
Colorless liquid The compound appears as a colorless liquid, which means it does not have any color when observed in its pure form.
Odor
Faint, specific odor The compound has a weak, distinct smell that can be detected at low concentrations.
Uses
Organic synthesis, pharmaceuticals, and agrochemicals 1H-Pyrrole-1-acetic acid, alpha-methyl-, methyl ester (9CI) is used as a key intermediate in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals.
Chemical properties and reactivity
The compound exhibits specific chemical properties and reactivity, making it an important compound in the field of organic chemistry. This includes its ability to undergo various chemical reactions, such as esterification, amidation, and other transformations.
Check Digit Verification of cas no
The CAS Registry Mumber 130016-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,0,1 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 130016-69:
(8*1)+(7*3)+(6*0)+(5*0)+(4*1)+(3*6)+(2*6)+(1*9)=72
72 % 10 = 2
So 130016-69-2 is a valid CAS Registry Number.
130016-69-2Relevant articles and documents
HCV NS5B polymerase inhibitors 2: Synthesis and in vitro activity of (1,1-dioxo-2H-[1,2,4]benzothiadiazin-3-yl) azolo[1,5-a]pyridine and azolo[1,5-a]pyrimidine derivatives
Wang, Guangyi,Lei, Huoxing,Wang, Xiaofang,Das, Debasis,Hong, Jian,Mackinnon, Colin H.,Coulter, Thomas S.,Montalbetti, Christian A.G.N.,Mears, Richard,Gai, Xinjie,Bailey, Sarah E.,Ruhrmund, Donald,Hooi, Lisa,Misialek, Shawn,Rajagopalan, P.T. Ravi,Cheng, Robert K.Y.,Barker, John J.,Felicetti, Brunella,Schoenfeld, Dorian L.,Stoycheva, Antitsa,Buckman, Brad O.,Kossen, Karl,Seiwert, Scott D.,Beigelman, Leonid
scheme or table, p. 4480 - 4483 (2010/04/05)
(1,1-dioxo-2H-[1,2,4]benzothiadiazin-3-yl) azolo[1,5-a]pyridine and azolo[1,5-a]pyrimidine derivatives have been investigated as potential anti-HCV drugs. Their synthesis, HCV NS5B polymerase inhibition, and replicon activity are discussed.
THE ALKYLATION OF METHYL 2-(1-PYRROLYL)ACETATE. A NEW SYNTHETIC METHOD OF α-AMINO ACIDS
Kashima, Choji,Maruyama, Tatsuya
, p. 1727 - 1730 (2007/10/02)
The alkylation of 2-(1-pyrrolyl)acetates was accomplished by the treatment with alkyl halides in the presence of LDA to give 2-(1-pyrrolyl)alkanoates, which were convertible into α-amino acids by ozonolysis.