66938-33-8 Usage
Uses
Used in Pharmaceutical Industry:
(4-BROMO-2-THIENYL)(4-METHOXYPHENYL)METHANONE is used as a building block for the synthesis of various pharmaceuticals due to its unique structure and potential biological activities.
Used in Agrochemical Industry:
(4-BROMO-2-THIENYL)(4-METHOXYPHENYL)METHANONE is used as a building block for the synthesis of various agrochemicals, contributing to the development of effective and innovative products in this field.
Used in Research:
(4-BROMO-2-THIENYL)(4-METHOXYPHENYL)METHANONE is used as a ligand in the development of catalysts for organic reactions, aiding in the advancement of chemical research and the discovery of new reaction pathways.
Used in Anti-inflammatory Applications:
(4-BROMO-2-THIENYL)(4-METHOXYPHENYL)METHANONE is used as an anti-inflammatory agent due to its potential to alleviate inflammation and associated symptoms.
Used in Anti-cancer Applications:
(4-BROMO-2-THIENYL)(4-METHOXYPHENYL)METHANONE is used as an anti-cancer agent, potentially contributing to the development of new cancer treatments and therapies.
Used in Anti-bacterial Applications:
(4-BROMO-2-THIENYL)(4-METHOXYPHENYL)METHANONE is used as an anti-bacterial agent, potentially aiding in the development of new antibiotics and treatments for bacterial infections.
Check Digit Verification of cas no
The CAS Registry Mumber 66938-33-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,9,3 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 66938-33:
(7*6)+(6*6)+(5*9)+(4*3)+(3*8)+(2*3)+(1*3)=168
168 % 10 = 8
So 66938-33-8 is a valid CAS Registry Number.
66938-33-8Relevant academic research and scientific papers
Synthesis and anthelminthic acitivity of alkyl-(5-acyl-1-benzimidazol-2-yl) carbamates
Raeymackers,Van Gelder,Roevens,Janssen
, p. 586 - 594 (2007/10/05)
A series of alkyl-(5-acyl-l-H-benzimidazol-2-yl)-carbamates were prepared and screened for anthelminthic activity. Some of them were found to be fully active at low, atoxic oral dose levels against gastro-intestinal nematodes. The activity against Syphacia muris and Strongyloides ratta is indicated. From these studies methyl (5-benzoyl-1-H-benzimidazol-2-yl) carbamate (mebendazole) and methyl [5-(4-fluorobenzoyl)-1-H-benzimidazol-2-yl]carbamate (flubendazole) were selected for detailed investigation.
