79685-43-1 Usage
Pyrimidine derivative
A compound based on the pyrimidine core structure, which is a six-membered heterocyclic aromatic ring containing four carbon atoms and two nitrogen atoms.
Benzylsulfonyl group
A functional group consisting of a benzyl group (a phenyl ring attached to a methylene group) connected to a sulfonyl group (a sulfur atom double-bonded to two oxygen atoms).
Chlorine atom
A halogen element present in the compound, which is known for its reactivity and ability to form various derivatives.
Biological activity
The compound has potential applications in medicinal chemistry and drug development due to its ability to interact with biological systems, such as enzymes, receptors, or other biomolecules.
Building block in synthesis
2-(benzylsulfonyl)-5-chloropyrimidine can be used as a starting material or intermediate in the synthesis of other organic compounds, making it a valuable component in organic chemistry.
Research and industrial applications
The compound's structure and properties make it useful for a variety of purposes, including as a research tool or in the development of new materials and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 79685-43-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,8 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79685-43:
(7*7)+(6*9)+(5*6)+(4*8)+(3*5)+(2*4)+(1*3)=191
191 % 10 = 1
So 79685-43-1 is a valid CAS Registry Number.
79685-43-1Relevant academic research and scientific papers
Pyrimidine-2-sulphides and their S-oxides for use in medicine and methods of use therefor, pharmaceutical compositions containing them, processes for their preparation and per se novel sulphides and S-oxides
-
, (2008/06/13)
Compounds of the formula STR1 (wherein X represents a halogen atom; n is 0, 1 or 2; R1 and R2, which may be the same or different, each represents a hydrogen atom or a carboxyl, esterified carboxyl, amido or mono- or di-C1-4 alkylamido group or a C1-4 alkyl group which may if desired carry a carboxyl or esterified carboxyl group; and R3 represents a C1-32 saturated or unsaturated, straight or branched, cyclic or acyclic aliphatic group or an araliphatic or heterocyclic substituted aliphatic group, a heterocyclic group or an aryl group which groups may if desired carry one or more substituents selected from halogen atoms and oxo, nitro, hydroxy, etherified hydroxy, esterified hydroxy, primary, secondary or tertiary amino, acylamino etherified mercapto or S=O or --SO2 derivatives thereof and esterified phosphonic acid groups) and, where an acidic or basic group is present, physiologically compatible salts thereof have been found to be of use in combating abnormal cell proliferation. The compounds are prepared inter alia by oxidation of the corresponding sulfide, displacement of a leaving atom or group from the 2-position of the pyrimidine by reaction with a sulfinic acid or by ring closure of the pyrimidine ring.
