87538-71-4 Usage
Description
(6Z)-6-[2-amino-5-(4-methoxyphenyl)pyrimidin-4(3H)-ylidene]cyclohexa-2,4-dien-1-one is a pyrimidine derivative with a molecular formula of C17H15N3O2. It features a cyclohexa-2,4-dien-1-one moiety, an amino group, and a methoxyphenyl group. (6Z)-6-[2-amino-5-(4-methoxyphenyl)pyrimidin-4(3H)-ylidene]cyclohexa-2,4-dien-1-one may hold potential pharmaceutical or biological applications due to its unique structure and composition, and further research could reveal its properties and possible uses.
Uses
Used in Pharmaceutical Industry:
(6Z)-6-[2-amino-5-(4-methoxyphenyl)pyrimidin-4(3H)-ylidene]cyclohexa-2,4-dien-1-one is used as a potential pharmaceutical compound for its possible applications in drug development. Its unique structure, which includes a pyrimidine core, a cyclohexa-2,4-dien-1-one moiety, and functional groups like an amino group and a methoxyphenyl group, may contribute to its interaction with biological targets, making it a candidate for further research and development in the pharmaceutical field.
Used in Biological Research:
In the field of biological research, (6Z)-6-[2-amino-5-(4-methoxyphenyl)pyrimidin-4(3H)-ylidene]cyclohexa-2,4-dien-1-one may serve as a valuable compound for studying its interactions with various biological systems. Its structure and composition could provide insights into its potential roles in biological processes, offering opportunities for new discoveries and applications in understanding complex biological mechanisms.
Check Digit Verification of cas no
The CAS Registry Mumber 87538-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,3 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 87538-71:
(7*8)+(6*7)+(5*5)+(4*3)+(3*8)+(2*7)+(1*1)=174
174 % 10 = 4
So 87538-71-4 is a valid CAS Registry Number.
87538-71-4Relevant articles and documents
Pot-economic synthesis of diarylpyrazoles and pyrimidines involving Pd-catalyzed cross-coupling of 3-trifloxychromone and triarylbismuth
Kumar, Abhijeet,Rao, Maddali L N
, (2018/12/10)
Abstract: The present study reveals the formation of 3,4-diarylpyrazole and 4,5-diarylpyrimidine in one-pot operation starting from 3-trifloxychromone and triarylbismuth. The complete process encompasses two steps in the one-pot operation. The first step leads to the formation of isoflavone via cross-coupling reaction of 3-trifloxychromone and triarylbismuth as a threefold arylating reagent. These isoflavones were further converted into 3,4-diarylpyrazole and 4,5-diarylpyrimidine using hydrazine hydrate and guanidinium chloride in the successive step in the same pot. Interestingly the formation of 3,4-diarylpyrazole was achieved in the shortest reaction time i.e., 30 min that too at room temperature. Overall the developed methodology provides easy access to the medicinally important diarylpyrazole and pyrimidine moiety in one-pot operation and in short reaction time. Graphical Abstract: Synopsis The work presented here describes the novel methodology for the formation of medicinally important heterocycles 3,4-diarylpyrazole and 4,5-diarylpyrimidine in one-pot operation starting from 3-trifloxychromone and triarylbismuth.
The reaction of amines with isoflavones. I. Formation of phenolic pyrimidines
Oluwadiya
, p. 1111 - 1112 (2007/10/02)
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