134703-37-0 Usage
Methyl ester derivative
1H-pyrrole-1-acetic acid The compound is derived from 1H-pyrrole-1-acetic acid by attaching a methyl ester group.
Methylene group
at the alpha position of the carboxylic acid A methylene group (CH2) is present at the alpha position, which is the carbon atom adjacent to the carboxylic acid group in the molecule.
Application
Organic synthesis and medicinal chemistry The compound is used as a building block in the synthesis of various pharmaceuticals and biologically active compounds.
Use as a reagent
Formation of carbon-carbon and carbon-nitrogen bonds 1H-Pyrrole-1-acetic acid, alpha-methylene-, methyl ester (9CI) is used in chemical reactions to facilitate the formation of carbon-carbon and carbon-nitrogen bonds.
Anti-inflammatory properties
Studies have shown that the compound possesses anti-inflammatory properties, which may be useful in the development of new drugs for treating inflammation-related conditions.
Anti-cancer properties
The compound has also been found to have anti-cancer properties, making it a promising candidate for the development of new cancer treatments.
Safety precautions
As with all chemical compounds, 1H-Pyrrole-1-acetic acid, alpha-methylene-, methyl ester (9CI) should be handled and used with proper care and safety measures to avoid potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 134703-37-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,7,0 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 134703-37:
(8*1)+(7*3)+(6*4)+(5*7)+(4*0)+(3*3)+(2*3)+(1*7)=110
110 % 10 = 0
So 134703-37-0 is a valid CAS Registry Number.
134703-37-0Relevant academic research and scientific papers
Yavari, Issa,Norouzi-Arasi, Hassan
, p. 87 - 92 (2002)
The α-addition of NH-acids such as pyrrole, indole, imidazole, or benzimidazole to methyl or ethyl propiolate proceeds under neutral conditions in the presence of a catalytic amount of triphenylphosphine to give the corresponding α-substituted alkyl acryl
