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CAS 80745-07-9

:

4-methoxy-2,3,6-trimethylbenzene-sulfonyl chloride

Description:
4-Methoxy-2,3,6-trimethylbenzene-sulfonyl chloride, also known by its CAS number 80745-07-9, is an organic compound characterized by the presence of a sulfonyl chloride functional group attached to a substituted aromatic ring. This compound features a methoxy group and three methyl groups on the benzene ring, contributing to its hydrophobic nature and influencing its reactivity. The sulfonyl chloride group is known for its high reactivity, particularly in nucleophilic substitution reactions, making this compound useful in organic synthesis, especially for the introduction of sulfonyl groups into other molecules. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of the methoxy group can enhance solubility in organic solvents, while the sulfonyl chloride functionality allows for the formation of sulfonamides and other derivatives. As with many sulfonyl chlorides, it is important to handle this compound with care due to its potential to release hydrochloric acid upon reaction and its reactivity towards moisture.
Formula:C10H13ClO3S
InChI:InChI=1/C10H13ClO3S/c1-6-5-9(14-4)7(2)8(3)10(6)15(11,12)13/h5H,1-4H3
SMILES:Cc1cc(c(C)c(C)c1S(=O)(=O)Cl)OC
Synonyms:
  • 4-Methoxy-2,3,6-trimethylbenzenesulphonyl chloride
  • 4-Methoxy-2,3,6-Trimethylbenzenesulfonyl Chloride
  • MTR CHLORIDE
  • MTR-CL
  • 4-METHOXY-2,3,6-TRIMETHYLBENZENE-
  • 4-METHOXY-2,3,6-TRIMETHYLPHENYLSULFONYL CHLORIDE
  • 4-METHOXY-2,3,6-TRIMETHYLBENZENE-SULFONYL CHLORIDE 97+%
  • 4-METHOXY-2,3,6-TRIMETHYLBENZENESULFONYL CHLORIDE: TECH., 90%
  • Benzenesulfonyl chloride, 4-methoxy-2,3,6-trimethyl-(9CI)
  • 4-Methoxy-2,3,6-trimethylphenylaulfomyl chloride
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