60722-70-5 Usage
Heterocyclic compound
Pyrimidine ring with a benzylsulfanyl group
The compound is classified as a heterocyclic compound because it contains a pyrimidine ring, which is a heterocyclic aromatic ring consisting of two carbon atoms and two nitrogen atoms, with a benzylsulfanyl group (a benzene ring with a sulfur atom attached to an alkyl chain) attached to it.
Pharmaceutical industry use
Intermediate for drug synthesis
2-(benzylsulfanyl)pyrimidin-4-amine is commonly used in the pharmaceutical industry as an intermediate compound in the synthesis of various drugs, making it a valuable building block for drug development.
Potential biological activities
Anti-cancer and anti-inflammatory properties
The compound has been studied for its potential biological activities, which include anti-cancer properties (ability to inhibit or prevent the growth and spread of cancer cells) and anti-inflammatory properties (ability to reduce inflammation in the body).
Structure and reactivity
Valuable for developing new chemical entities
The unique structure and reactivity of 2-(benzylsulfanyl)pyrimidin-4-amine make it a valuable building block for the development of new chemical entities with potential medicinal uses, as it can be modified or combined with other compounds to create new drugs with desired therapeutic effects.
Check Digit Verification of cas no
The CAS Registry Mumber 60722-70-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,7,2 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 60722-70:
(7*6)+(6*0)+(5*7)+(4*2)+(3*2)+(2*7)+(1*0)=105
105 % 10 = 5
So 60722-70-5 is a valid CAS Registry Number.
60722-70-5Relevant articles and documents
Process for synthesis of cytosine
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Paragraph 0010; 0019, (2017/05/05)
The invention discloses a process for synthesizing cytosine. A 3-hydroxyacrylonitrile compound and an O-methylisourea compound or an S-methylisothiourea compound or an S-ethylisothiourea compound or an S-benzylisothiourea compound are used as raw materials. The process comprises the steps of adding a catalyst and an organic solvent into a reaction kettle, stirring, and then adding the raw materials; heating the mixture to be 50-90 DEG C, and reacting for 8-12 hours; evaporating the solvent to obtain an intermediate; adding concentrated hydrochloric acid into the intermediate, heating to be 70-100 DEG C, and preserving the heat for 1-2 hours; adding water, performing hot filtration, and cooling the obtained filtrate to room temperature; dripping a sodium hydroxide solution into the filtrate to adjust the pH value to be 7-7.5, and cooling to 10-15 DEG C; filtering after cooling, washing, and drying to obtain the cytosine. The process has the advantages that the process steps are simple, the production period is short, and the cost is low; the conversion rate of the raw materials is high, and the synthesized product is good in quality and high in yield, so that the process is suitable for industrialized production.
