6292-55-3 Usage
Uses
Used in Research and Development:
3-Acetylaminfluorene is used as a research tool for investigating the mechanisms of chemical carcinogenesis, aiding in the development of new cancer treatments. Its potent carcinogenic properties make it a valuable agent for studying the processes that lead to the formation of tumors.
Used in Cancer Treatment Development:
In the field of oncology, 3-acetylaminofluorene is utilized as a test compound to evaluate the effectiveness of potential cancer treatments. It helps researchers understand how different therapeutic agents may counteract or mitigate the carcinogenic effects of such compounds.
Used in Chemoprevention Studies:
3-Acetylaminfluorene is employed as a benchmark in chemoprevention studies to assess the efficacy of agents designed to inhibit tumor formation. By observing the impact of these agents on the compound's carcinogenic effects, researchers can determine their potential as preventive measures against cancer.
Used in Regulatory and Safety Assessments:
Due to its hazardous nature, 3-acetylaminofluorene is also used in regulatory settings to establish safety standards and guidelines for research and industrial applications, ensuring that exposure to 3-acetylaminofluorene is minimized and controlled.
Used in Toxicology and Environmental Studies:
3-Acetylaminfluorene is applied in toxicology to study the effects of exposure to carcinogens on biological systems. It is also used in environmental studies to understand the impact of such substances on ecosystems and to develop methods for their detection and mitigation.
Check Digit Verification of cas no
The CAS Registry Mumber 6292-55-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6292-55:
(6*6)+(5*2)+(4*9)+(3*2)+(2*5)+(1*5)=103
103 % 10 = 3
So 6292-55-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H13NO/c1-10(17)16-13-7-6-12-8-11-4-2-3-5-14(11)15(12)9-13/h2-7,9H,8H2,1H3,(H,16,17)
6292-55-3Relevant academic research and scientific papers
A novel construction of acetamides from rhodium-catalyzed aminocarbonylation of DMC with nitro compounds
Bao, Zhi-Peng,Miao, Ren-Guan,Qi, Xinxin,Wu, Xiao-Feng
supporting information, p. 1955 - 1958 (2021/03/02)
Dimethyl carbonate (DMC), an environment-friendly compound prepared from CO2, shows diverse reactivities. In this communication, an efficient procedure using DMC as both a C1 building block and solvent in the aminocarbonylation reaction with nitro compounds has been developed. W(CO)6acts both a CO source and a reductant here.
Synthesis of Fluorenes Starting from 2-Iodobiphenyls and CH2Br2 through Palladium-Catalyzed Dual C-C Bond Formation
Shi, Guangfa,Chen, Dushen,Jiang, Hang,Zhang, Yu,Zhang, Yanghui
, p. 2958 - 2961 (2016/07/06)
A facile and efficient approach is developed for the synthesis of fluorene and its derivatives starting from 2-iodobiphenyls and CH2Br2. A range of fluorene derivatives can be synthesized under relatively mild conditions. The reaction proceeds via a tandem palladium-catalyzed dual C-C bond formation sequence through the key dibenzopalladacyclopentadiene intermediates, which are obtained from 2-iodobiphenyls through palladium-catalyzed C-H activation.
