80254-36-0 Usage
Molecular Weight
284.44 g/mol
Pyrimidine ring
A six-membered heterocyclic ring with four carbon atoms and two nitrogen atoms.
Methyl groups
Three methyl groups (CH3) are attached to the pyrimidine ring at positions 1, 3, and 6.
Methyl groups
Provide steric hindrance and can influence the compound's reactivity and physical properties.
Amino group
An amino group (NH2) is attached to the phenyl group, which is connected to the pyrimidine ring at position 5.
Amino group
Can participate in various chemical reactions, such as acylation, alkylation, and formation of salts.
Phenyl group
A phenyl group (C6H5) is connected to the amino group.
Phenyl group
Adds aromaticity and can influence the compound's stability, reactivity, and physical properties.
Dithione groups
Two dithione groups (CS2) are attached to positions 2 and 4 of the pyrimidine ring.
Dithione groups
Provide sulfur-based reactivity and can undergo various reactions, such as nucleophilic substitution and redox reactions.
Pyrimidine
A heterocyclic compound with potential applications in pharmaceuticals and agrochemicals.
Intermediate in the synthesis of other organic compounds
Due to its complex structure, it can be used as a building block for the synthesis of more complex molecules.
Pharmaceutical industry
The pyrimidine ring is a common structural motif in many pharmaceuticals, and this compound may have potential applications in drug development.
Chemical industry
The compound's unique structure and reactivity may be useful in the development of new materials or chemical processes.
Nucleophilic substitution
The dithione groups can undergo nucleophilic substitution reactions with various nucleophiles.
Electrophilic aromatic substitution
The phenyl group can undergo electrophilic aromatic substitution reactions, such as halogenation, nitration, and sulfonation.
Redox reactions
The dithione groups can participate in redox reactions, potentially acting as reducing agents.
Thermal stability
The compound's stability under heat may depend on the specific functional groups and their interactions.
Chemical stability
The compound's stability in the presence of other chemicals, such as acids, bases, or oxidizing agents, may vary depending on the reactivity of its functional groups.
Solubility
The solubility of the compound in various solvents (e.g., water, organic solvents) may depend on the polarity and hydrogen bonding capabilities of its functional groups.
Further Research
Additional studies and experimentation are needed to fully understand the compound's properties, reactivity, and potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 80254-36-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,5 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 80254-36:
(7*8)+(6*0)+(5*2)+(4*5)+(3*4)+(2*3)+(1*6)=110
110 % 10 = 0
So 80254-36-0 is a valid CAS Registry Number.
80254-36-0Relevant articles and documents
TETRAHYDRO-1,2,3,4 PYRIMIDINES ET OCTAHYDRO-1,2,3,4,5,6,7,8 QUINAZOLINES DITHIONES-2,4 ET DIONES-2,4 SYNTHESE ET ETUDE DU MECANISME
Lamazouere, A. M.,Sotiropoulos, J.
, p. 2451 - 2458 (2007/10/02)
A synthesis of tetrahydropyrimidine-dithiones and octahydroquinazoline-dithiones has been realized by direct action, in basic media, of alkyl or aryl isothiocyanates on ketones possessing at least an hydrogen atom in an α-position.The clarification of the complex mechanism of this reaction has been attempted.It is possible to reach corresponding diones by desulphurization of the dithiones.
