101587-85-3 Usage
Uses
Used in Pharmaceutical Industry:
1-(6-HYDROXY-3,6-DIMETHYL-4-PHENYL-4,5,6,7-TETRAHYDRO-2H-INDAZOL-5-YL)-ETHANONE is used as a building block for the synthesis of various pharmaceutical compounds due to its versatile reactivity and functionality. Its unique molecular structure allows for the creation of a wide range of therapeutic agents.
Used in Organic Chemistry:
In the field of organic chemistry, 1-(6-HYDROXY-3,6-DIMETHYL-4-PHENYL-4,5,6,7-TETRAHYDRO-2H-INDAZOL-5-YL)-ETHANONE serves as a key intermediate for the synthesis of complex organic molecules. Its diverse functional groups facilitate numerous chemical reactions, contributing to the development of novel organic compounds.
Used in Medicinal Chemistry and Drug Discovery Research:
1-(6-HYDROXY-3,6-DIMETHYL-4-PHENYL-4,5,6,7-TETRAHYDRO-2H-INDAZOL-5-YL)-ETHANONE may possess pharmacological or biological activities that are of interest in medicinal chemistry and drug discovery research. Its unique molecular structure and potential applications make it a valuable chemical for exploring new therapeutic avenues and developing innovative drugs.
Used in Chemical Research and Development:
1-(6-HYDROXY-3,6-DIMETHYL-4-PHENYL-4,5,6,7-TETRAHYDRO-2H-INDAZOL-5-YL)-ETHANONE's properties and potential applications also make it a valuable asset in the field of chemical research and development. It can be utilized in the design and synthesis of new materials, catalysts, and other advanced chemical products, contributing to the advancement of various scientific and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 101587-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,5,8 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 101587-85:
(8*1)+(7*0)+(6*1)+(5*5)+(4*8)+(3*7)+(2*8)+(1*5)=113
113 % 10 = 3
So 101587-85-3 is a valid CAS Registry Number.
101587-85-3Relevant academic research and scientific papers
SYNTHESIS AND BIOLOGICAL ACTIVITY OF SUBSTITUTED 7-AZA-8-AZA(OXA)-BICYCLO-6,9-NONADIENES
Smirnova, N. O.,Plotnikov, O. P.,Vinogradova, N. A.,Sorokin, V. V.,Kriven'ko, A. P.
, p. 49 - 50 (2007/10/03)
Hydroxylamine- and hydrazine-induced heterocyclization of readily available 5-hydroxy-2,4-diacetyl-5-methyl-3-R-cyclohexanones (R = methyl, phenyl, m-nitrophenyl, α-furyl) yielded 6-acetyl-5-hydroxy-5,9-dimethyl-7-R-1-aza(oxa)-2-azabicyclo-2,8-nona
