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CAS 6461-30-9

:

5-Pyrimidinesulfonyl chloride, 1,2,3,4-tetrahydro-6-methyl-2,4-dioxo-

Description:
5-Pyrimidinesulfonyl chloride, 1,2,3,4-tetrahydro-6-methyl-2,4-dioxo- is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered heterocyclic aromatic ring containing nitrogen atoms. This compound features a sulfonyl chloride functional group, which is known for its reactivity and ability to act as a sulfonating agent. The presence of the tetrahydro structure indicates that it has a saturated cyclic component, contributing to its stability and solubility in various solvents. The dioxo groups suggest that it has two carbonyl functionalities, which can participate in various chemical reactions, including nucleophilic attacks. This compound is typically used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to form covalent bonds with nucleophiles. Its reactivity, combined with the unique structural features, makes it a valuable intermediate in synthetic chemistry. Safety precautions should be taken when handling this compound, as sulfonyl chlorides can be corrosive and may release toxic gases upon reaction with water or moisture.
Formula:C5H5ClN2O4S
InChI:InChI=1/C5H5ClN2O4S/c1-2-3(13(6,11)12)4(9)8-5(10)7-2/h1H3,(H2,7,8,9,10)
InChI key:InChIKey=XDXYTKIQVSJRIX-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C1=C(C)NC(=O)NC1=O
Synonyms:
  • 1,2,3,4-Tetrahydro-6-methyl-2,4-dioxo-5-pyrimidinesulfonyl chloride
  • 2,4-Dihydroxy-6-methylpyrimidine-5-sulfonyl chloride
  • 5-Pyrimidinesulfonyl chloride, 2,4-dihydroxy-6-methyl-
  • 6-Methyl-2,4-Dioxo-1,2,3,4-Tetrahydropyrimidine-5-Sulfonyl Chloride
  • 6-Methyluracil-5-sulfochloride
  • 6-Methyluracil-5-sulfonyl chloride
  • NSC 46425
  • 5-Pyrimidinesulfonyl chloride, 1,2,3,4-tetrahydro-6-methyl-2,4-dioxo-
  • AKOS MSC-0121
  • 1,2,3,4-Tetrahydro-6-methyl-2,4-dioxo-5-pyrimidinesulfonyl
  • See more synonyms
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