3807-58-7 Usage
Uses
Used in Organic Synthesis:
1-(4-METHOXYPHENYL)-2,5-DIMETHYL-1H-PYRROLE-3-CARBOXYLIC ACID is used as a building block for the synthesis of various organic compounds due to its unique structural features and functional groups.
Used in Medicinal Chemistry:
1-(4-METHOXYPHENYL)-2,5-DIMETHYL-1H-PYRROLE-3-CARBOXYLIC ACID is used as a starting material for the development of pharmaceuticals and other biologically active molecules, leveraging its versatile chemical properties and potential for further modification.
Used in Pharmaceutical Industry:
1-(4-METHOXYPHENYL)-2,5-DIMETHYL-1H-PYRROLE-3-CARBOXYLIC ACID is used as a key intermediate in the synthesis of drugs, contributing to the discovery and development of new therapeutic agents.
Used in Chemical Research and Development:
1-(4-METHOXYPHENYL)-2,5-DIMETHYL-1H-PYRROLE-3-CARBOXYLIC ACID is used as a valuable compound in chemical research, enabling the exploration of new chemical reactions and the creation of novel molecular structures with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 3807-58-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,0 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3807-58:
(6*3)+(5*8)+(4*0)+(3*7)+(2*5)+(1*8)=97
97 % 10 = 7
So 3807-58-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H15NO3/c1-9-8-13(14(16)17)10(2)15(9)11-4-6-12(18-3)7-5-11/h4-8H,1-3H3,(H,16,17)
3807-58-7Relevant academic research and scientific papers
Novel pyrrole- and 1,2,3-triazole-based 2,3-oxidosqualene cyclase inhibitors
Watanabe, Takumi,Umezawa, Yoji,Takahashi, Yoshikazu,Akamatsu, Yuzuru
scheme or table, p. 5807 - 5810 (2010/11/24)
Pyrrole- and 1,2,3-triazole-based 2,3-oxidosqualene cyclase (OSC) inhibitors 3 and 4 were discovered by conducting a virtual screening, a docking study based on the crystallographic structure of OSC, and biological assays. The hit rate of the assays was increased by establishing appropriate substructural filters in the virtual screening stage. Amide derivatives of 8 and 12 preserved the inhibitory activity of parent compound 3, which provided a reasonable starting point for further structure-activity-relationship (SAR) studies on related compounds.
