Interesting facts
Interesting Facts About Methyl Trifluoromethanesulfonate
Methyl trifluoromethanesulfonate is a fascinating compound that belongs to the category of sulfonates. Here are some key insights into its properties and applications:
- Unique Structure: This compound features a trifluoromethanesulfonate functional group, which contributes to its reactivity. The presence of fluorine atoms makes it a strong electrophile.
- Versatile Reagent: Methyl trifluoromethanesulfonate is widely utilized in organic synthesis, particularly as a reagent for various transformations. It is known for its ability to act as an effective methylating agent.
- High Reactivity: Due to the electronegativity of the fluorine atoms, this compound can engage in nucleophilic substitution reactions, making it valuable in producing methyl ethers and other derivatives.
- Role in Pharmaceutical Chemistry: In the pharmaceutical industry, it is employed for the synthesis of complex molecules. Its ability to add methyl groups efficiently is particularly advantageous in drug development.
- Environmental Considerations: Given its fluoroalkyl nature, care must be taken in handling methyl trifluoromethanesulfonate due to potential environmental and health impacts. A comparison with similar compounds helps understand its behavior.
As one studies this compound, one might ponder the question: How does this compound compare to other sulfonate esters in reactivity? The chemistry of methyl trifluoromethanesulfonate not only showcases a rich field of study but also emphasizes the importance of careful application in scientific research and industry.
Synonyms
Methyl trifluoromethanesulfonate
333-27-7
Methyl triflate
Methyl trifluoromethanesulphonate
Methanesulfonic acid, trifluoro-, methyl ester
Methyl trifluoromethane sulfonate
MeOTf
CCRIS 1158
Trifluoromethanesulfonic Acid Methyl Ester
EINECS 206-371-7
UNII-7B25Z22EPV
NSC 270679
7B25Z22EPV
DTXSID6049272
AI3-62911
NSC-270679
DTXCID1029128
1,1,1-Trifluoromethanesulfonic acid methyl ester
Methanesulfonic acid, 1,1,1-trifluoro-, methyl ester
trifluoro-methanesulfonic acid methyl ester
METHYL TRIFLUOROMETHANESULFONATE [MI]
C2H3F3O3S
METHYLTRIFLUOROMETHANESULFONATE
methyltriflate
methyl trifiate
TfOMe
MFCD00000409
triflic acid methyl ester
CF3SO2OCH3
SCHEMBL38490
Methyl trifloromethanesulfonate
Methyl trifluoromethylsulfonate
methyltrifluoromethane sulfonate
methyl trifluoromethane-sulfonate
CHEMBL3185488
BCP22549
CS-B0882
Tox21_202914
FD2053
NSC270679
AKOS005063680
FM34989
trifluoro-methansulfonic acid methylester
Trifluoromethylsulfonic acid methyl ester
Methyl trifluoromethanesulfonate, >=98%
NCGC00260460-01
AS-18305
BP-21280
CAS-333-27-7
DB-030038
Methanesulfonic acid, trifluoro, methyl ester
NS00022063
T2029
EN300-62786
Q907614
Methanesulfonic acid, 1,1,1trifluoro, methyl ester
F1905-7179
Methyl trifluoromethanesulfonate, for GC derivatization, 98.0%
Solubility of Methyl Trifluoromethanesulfonate
Methyl trifluoromethanesulfonate, with the chemical formula CH3CF3SO3CH3, exhibits interesting solubility characteristics due to its unique molecular structure. This compound is generally soluble in a variety of solvents, which can be summarized as follows:
As stated, “the solubility of a compound is a reflection of its molecular interactions,” which is particularly evident here. Understanding the solubility of methyl trifluoromethanesulfonate is crucial for its applications in chemical synthesis and industrial processes.