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4-amino-2-[4-(1-methylethyl)phenyl]-5H-chromeno[4,3-d]pyrimidin-5-one is a complex organic compound with a molecular formula of C18H16N4O2. It is a derivative of chromeno[4,3-d]pyrimidin-5-one, featuring a 4-amino group and a 4-(1-methylethyl)phenyl substituent. 4-amino-2-[4-(1-methylethyl)phenyl]-5H-chromeno[4,3-d]pyrimidin-5-one is characterized by its unique structure, which includes a chromeno[4,3-d]pyrimidin-5-one core, a 4-amino group, and a 4-(1-methylethyl)phenyl group attached to the core. It is a heterocyclic compound with potential applications in medicinal chemistry and pharmaceutical research, particularly in the development of new drugs and therapeutic agents. The compound's specific properties, such as solubility, stability, and reactivity, can be influenced by the presence of these functional groups and the overall molecular structure.

6053-78-7

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6053-78-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6053-78-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6053-78:
(6*6)+(5*0)+(4*5)+(3*3)+(2*7)+(1*8)=87
87 % 10 = 7
So 6053-78-7 is a valid CAS Registry Number.

6053-78-7Downstream Products

6053-78-7Relevant academic research and scientific papers

Resonance energy of diradicals - 1,8-naphthoquinodimethane

Roth, Wolfgang R.,Unger, Christian,Wasser, Thorsten

, p. 2155 - 2169 (2007/10/03)

From the racemization of 19c and the temperature and NO dependence of the trapping rate of 20b between 218 and 288°C the energy profile for the equilibrium 19b ? 20b is derived. The singlet-triplet splitting of the diradical is 2.5 kcal · mol-1 with the triplet being the ground state. By comparison of the experimental reaction enthalpy with the analogous value for 25, 26 or a hypothetical model reaction with non-interacting radicals it is shown that the stabilizing interaction of the radicals in the singlet state of 20b is negligible making the stabilization of the triplet equivalent to the singlet-triplet splitting. By using literature data it is shown by an analogous analysis that the interaction of the radicals in the bisallyl diradical 28 and in the triplet state of the trimethylenmethane derivative 29 is also negligible whereas in the singlet state of 29 the interaction is strongly destabilizing. VCH Verlagsgesellschaft mbH, 1996.

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