39573-20-1 Usage
Description
(5-BROMO-2-METHYLAMINO-PHENYL)-PHENYL-METHANONE is a chemical compound characterized by its molecular formula C13H11BrNO. It is a ketone derivative featuring a phenyl group and a bromo-substituted 2-methylamino-phenyl group. (5-BROMO-2-METHYLAMINO-PHENYL)-PHENYL-METHANONE is known for its potential applications in the pharmaceutical industry and has been investigated for its biological activities, such as its role in cancer treatment and as an anti-inflammatory agent.
Uses
Used in Pharmaceutical Industry:
(5-BROMO-2-METHYLAMINO-PHENYL)-PHENYL-METHANONE is used as a building block for the synthesis of various drugs and pharmaceutical ingredients. Its unique structure and properties make it a valuable component in the development of new medications.
Used in Cancer Treatment Research:
In the field of cancer treatment, (5-BROMO-2-METHYLAMINO-PHENYL)-PHENYL-METHANONE is studied for its potential role in targeting and treating cancer cells. Its specific interactions with biological systems may contribute to the development of novel therapeutic strategies against cancer.
Used as an Anti-Inflammatory Agent:
(5-BROMO-2-METHYLAMINO-PHENYL)-PHENYL-METHANONE has also been explored for its anti-inflammatory properties, which could be beneficial in the treatment of various inflammatory conditions and diseases.
Used in Organic Synthesis:
As a reagent in organic synthesis, (5-BROMO-2-METHYLAMINO-PHENYL)-PHENYL-METHANONE is utilized for the creation of a wide range of chemical products, contributing to the advancement of chemical research and development.
Used in Medicinal Chemistry and Drug Discovery Research:
(5-BROMO-2-METHYLAMINO-PHENYL)-PHENYL-METHANONE's potential applications extend to medicinal chemistry and drug discovery research, where it may be employed to identify new drug candidates or optimize existing ones for improved efficacy and safety.
Check Digit Verification of cas no
The CAS Registry Mumber 39573-20-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,5,7 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 39573-20:
(7*3)+(6*9)+(5*5)+(4*7)+(3*3)+(2*2)+(1*0)=141
141 % 10 = 1
So 39573-20-1 is a valid CAS Registry Number.
39573-20-1Relevant articles and documents
Method for synthesizing 2-aminobenzophenone compound
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Paragraph 0074-0076, (2019/02/04)
The invention discloses a method for synthesizing a 2-aminobenzophenone compound, and belongs to the technical field of organic synthesis. According to the key point of the technical scheme, the method comprises the following steps that an N-nitroso-2-ami
Enantioselective Intramolecular Copper-Catalyzed Borylacylation
Whyte, Andrew,Burton, Katherine I.,Zhang, Jingli,Lautens, Mark
supporting information, p. 13927 - 13930 (2018/10/02)
An enantioselective copper-catalyzed intramolecular borylacylation is reported. The reaction proceeds through an initial enantioselective borylcupration of the styrene, followed by a nucleophilic attack on the tethered carbamoyl chloride. The products, chiral borylated 3,3-disubstituted oxindoles, were generated in excellent yields and enantioselectivities. The versatile carbon–boron bond provides a platform for a wide array of diversification.
Silica gel-mediated hydroamination/semipinacol rearrangement of 2-alkylaminophenylprop-1-yn-3-ols: Synthesis of 2-oxindoles from alkynes and 1-(2-aminophenyl) ketones
Susanti, Dewi,Ng, Linda Li Ru,Chan, Philip Wai Hong
supporting information, p. 353 - 358 (2014/05/20)
2-Alkylaminophenylprop-1-yn-3-ols, prepared from the lithium diisopropylamide (LDA)- mediated 1,2-addition of alkynes to 1-(2-aminophenyl) ketones, can be converted to 3,3-disubstituted 2-oxindoles by using silica gel in n-hexane/ ethyl acetate (20:1 v/v) as the reaction medium. The utility of the approach as a potential scale-up strategy for the synthesis of 2-oxindoles was exemplified by the large-scale synthesis of one adduct in excellent yield. The synthetic applicability of this chemistry was also demonstrated by the recycling of the silica gel up to 8 times with no apparent loss of activity being observed for the same example.
