3168-85-2 Usage
General Description
2-Methyl-1H-pyrrole-3-carboxylic acid methyl ester is a chemical compound with the molecular formula C7H9NO2. It is a methyl ester derivative of 2-methyl-1H-pyrrole-3-carboxylic acid and is a colorless liquid at room temperature. This chemical compound is commonly used in organic synthesis and pharmaceutical research, where it serves as a building block for the synthesis of various biologically active compounds. It has also been studied for its potential pharmacological properties, including anti-inflammatory and anti-cancer activities. Additionally, 2-Methyl-1H-pyrrole-3-carboxylic acid methyl ester may have applications in the development of new materials and chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 3168-85-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,6 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3168-85:
(6*3)+(5*1)+(4*6)+(3*8)+(2*8)+(1*5)=92
92 % 10 = 2
So 3168-85-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H9NO2/c1-5-6(3-4-8-5)7(9)10-2/h3-4,8H,1-2H3
3168-85-2Relevant articles and documents
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Eisner,U. et al.
, p. 357 - 361 (1972)
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Synthesis of functionalized pyrroles and 6,7-dihydro-1H-indol-4(5H)-ones by reaction of 1,3-dicarbonyl compounds with 2-azido-1,1-diethoxyethane
Bellur, Esen,Langer, Peter
, p. 2151 - 2154 (2007/10/03)
The condensation of 1,3-dicarbonyl compounds with 2-azido-1,1- diethoxyethane and subsequent cyclization allowed an efficient synthesis of a variety of pyrroles and 6,7-dihydro-1H-indol-4(5H)-ones.
Carbene and Silicon Routes toward a Simple Nitrile Ylide. Spectroscopic, Kinetic, and Chemical Characterization
Turro, Nicholas J.,Cha, Yuan,Gould, Ian R.,Padwa, Albert,Gasdaska, John R.,Tomas, Miguel
, p. 4415 - 4417 (2007/10/02)
The generation and characterization of methyl nitrile ylide photochemically by addition of singlet methylene to acetonitrile and chemically from silylthioimidate and subsequent dipolar cycloaddition are carried out.
