23856-15-7 Usage
Description
(5-nitro-1H-indazol-1-yl)(phenyl)methanone is a chemical compound with the molecular formula C14H9N3O3. It features a nitro group and a phenyl group attached to an indazole ring, which contributes to its potential biological and pharmacological activities.
Used in Pharmaceutical Research and Drug Development:
(5-nitro-1H-indazol-1-yl)(phenyl)methanone is used as a key intermediate in the synthesis of various pharmaceutical agents for its potential biological and pharmacological properties. It aids in the development of new drugs targeting a range of medical conditions.
Used in Cancer Treatment:
In the field of oncology, (5-nitro-1H-indazol-1-yl)(phenyl)methanone is used as a compound with potential anticancer properties, contributing to the development of novel therapeutics for cancer treatment.
Used in Inflammatory Disease Management:
(5-nitro-1H-indazol-1-yl)(phenyl)methanone is also utilized in the research and development of medications for inflammatory diseases, given its potential to modulate inflammatory pathways and provide therapeutic benefits.
Safety Note:
It is crucial to handle (5-nitro-1H-indazol-1-yl)(phenyl)methanone with care due to its potential hazards, and it should be used in compliance with established safety protocols to ensure the well-being of researchers and patients alike.
Check Digit Verification of cas no
The CAS Registry Mumber 23856-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,8,5 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23856-15:
(7*2)+(6*3)+(5*8)+(4*5)+(3*6)+(2*1)+(1*5)=117
117 % 10 = 7
So 23856-15-7 is a valid CAS Registry Number.
23856-15-7Relevant articles and documents
Selective N1-Acylation of Indazoles with Acid Anhydrides Using an Electrochemical Approach
DIssanayake, D.M.M. Mevan,Vannucci, Aaron K.
supporting information, p. 457 - 460 (2019/01/23)
An electrochemical synthesis method for the selective N1-acylation of indazoles has been developed. This "anion pool" approach electrochemically reduces indazole molecules generating indazole anions and H2. Acid anhydrides are then introduced to the solution resulting in selective acylation of the N1-position of the indazoles. This procedure can also be applied to the acylation of benzimidazoles and indoles. The reaction can also be performed using a 9 V battery without loss of reaction efficiency.
Reissert Compound Formation with Fused Five-Membered Ring Heterocycles
Uff, Barrie C.,Ho, Yee-Ping,Brown, David S.,Fisher, Ian,Popp, Frank D.,Kant, Joydeep
, p. 2652 - 2681 (2007/10/02)
Reissert compounds have been prepared in high yield from benzothiazole by use of trimethylsilyl cyanide as source of cyanide in a single phase system.Analogues have been made from benzoxazole, indazole and 1-methylindazole but the method was unsuccessful with 1,2-benzisoxazole and pyrazole.Conjugate base alkylation followed by removal of the Reissert grouping provides a route to 2-alkylbenzothiazoles and -benzoxazoles, and 3-alkylated indazoles.Efficient access to pyridobenzothiazole and benzothiazoloisoquinoline derivatives results from appropriate intramolecular cyclisations.A crystal structure determination of 3-benzoyl-2,3-dihydro-2-benzothiazolecarbonitrile is reported.
