66938-61-2 Usage
Uses
Used in Organic Synthesis:
(4-AMINO-3-NITRO-PHENYL)-(3-CHLORO-PHENYL)-METHANONE is used as an intermediate in the synthesis of various organic compounds due to its reactive functional groups and unique structure.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (4-AMINO-3-NITRO-PHENYL)-(3-CHLORO-PHENYL)-METHANONE is used as a building block for the development of new pharmaceuticals, potentially targeting specific biological receptors or enzymes.
Used in Materials Science:
(4-AMINO-3-NITRO-PHENYL)-(3-CHLORO-PHENYL)-METHANONE may also find applications in materials science, where its structural properties could be exploited to create novel materials with specific characteristics.
Safety Note:
It is crucial to handle (4-AMINO-3-NITRO-PHENYL)-(3-CHLORO-PHENYL)-METHANONE with care and adhere to proper safety protocols, as it may pose potential hazards due to its chemical nature.
Check Digit Verification of cas no
The CAS Registry Mumber 66938-61-2 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, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 66938-61:
(7*6)+(6*6)+(5*9)+(4*3)+(3*8)+(2*6)+(1*1)=172
172 % 10 = 2
So 66938-61-2 is a valid CAS Registry Number.
66938-61-2Relevant academic research and scientific papers
Synthesis of LIAZAL, a retinoic acid metabolism blocking agent (RAMBA) with potential clinical applications in oncology and dermatology.
Freyne,Raeymaekers,Venet,Sanz,Wouters,De Coster,Wauwe
, p. 267 - 272 (2007/10/03)
The synthesis of LIAZAL (compound 9, R085246) is described. LIAZAL inhibits all-trans-retinoic acid metabolism and thereby exerts retinoid-like effects in vivo.
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.
