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Details

Stereochemistry ACHIRAL
Molecular Formula C3H3F3O2
Molecular Weight 128.0499
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHYL(TRIFLUOROMETHYL)DIOXIRANE

SMILES

CC1(OO1)C(F)(F)F

InChI

InChIKey=NEGUMGNBGIFXAL-UHFFFAOYSA-N
InChI=1S/C3H3F3O2/c1-2(7-8-2)3(4,5)6/h1H3

HIDE SMILES / InChI

Molecular Formula C3H3F3O2
Molecular Weight 128.0499
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Concerning selectivity in the oxidation of peptides by dioxiranes. Further insight into the effect of carbamate protecting groups.
2010-07-16
Oxyfunctionalization of non-natural targets by dioxiranes. 6. On the selective hydroxylation of cubane.
2009-08-20
A facile synthesis of C-24 and C-25 oxysterols by in situ generated ethyl(trifluoromethyl)dioxirane.
2009-01
An investigation by means of correlation analysis into the mechanisms of oxidation of aryl methyl sulfides and sulfoxides by dimethyldioxirane in various solvents.
2008-02-21
Oxidation of peptides by methyl(trifluoromethyl)dioxirane: the protecting group matters.
2007-01-19
Oxidative cleavage of p-methoxybenzyl ethers with methyl(trifluoromethyl)dioxirane.
2005-10-13
Oxygenation of alkane C-H bonds with methyl(trifluoromethyl)dioxirane: effect of the substituents and the solvent on the reaction rate.
2005-09-30
Mechanism of the oxidation of sulfides by dioxiranes: conformational mobility and transannular interaction in the oxidation of thianthrene 5-oxide.
2004-12-24
Unexpectedly selective formation and reactions of epoxycyclooctenones under microwave-mediated conditions.
2004-04-15
Singlet-oxygen generation in the catalytic reaction of dioxiranes with nucleophilic anions.
2004-02
Epoxidation of chiral camphor N-enoylpyrazolidinones with methyl(trifluoromethyl)dioxirane and urea hydrogen peroxide/acid anhydride: reversal of stereoselectivity.
2003-12-12
Oxyfunctionalization of non-natural targets by dioxiranes. 5. Selective oxidation of hydrocarbons bearing cyclopropyl moieties.
2003-10-03
Relative reactivity of peracids versus dioxiranes (DMDO and TFDO) in the epoxidation of alkenes. A combined experimental and theoretical analysis.
2003-01-29
Mechanism of the oxidation of sulfides by dioxiranes. 1. Intermediacy of a 10-S-4 hypervalent sulfur adduct.
2002-08-07
Effect of geminal substitution on the strain energy of dioxiranes. Origin of the low ring strain of dimethyldioxirane.
2002-05-31
Oxyfunctionalization of non-natural targets by dioxiranes. 4. Efficient oxidation of Binor S using methyl(trifluoromethyl)dioxirane.
2001-12-28
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 22:24:51 GMT 2025
Edited
by admin
on Mon Mar 31 22:24:51 GMT 2025
Record UNII
A7JNM906ZN
Record Status Validated (UNII)
Record Version
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Name Type Language
METHYL(TRIFLUOROMETHYL)DIOXIRANE
MI  
Systematic Name English
METHYL(TRIFLUOROMETHYL)DIOXIRANE [MI]
Preferred Name English
TRIFLUOROMETHYL(METHYL)DIOXIRANE
Systematic Name English
1-METHYL-1-(TRIFLUOROMETHYL)DIOXIRANE
Systematic Name English
DIOXIRANE, METHYL(TRIFLUOROMETHYL)-
Systematic Name English
Code System Code Type Description
MERCK INDEX
m7475
Created by admin on Mon Mar 31 22:24:51 GMT 2025 , Edited by admin on Mon Mar 31 22:24:51 GMT 2025
PRIMARY Merck Index
CAS
115464-59-0
Created by admin on Mon Mar 31 22:24:51 GMT 2025 , Edited by admin on Mon Mar 31 22:24:51 GMT 2025
PRIMARY
PUBCHEM
11051663
Created by admin on Mon Mar 31 22:24:51 GMT 2025 , Edited by admin on Mon Mar 31 22:24:51 GMT 2025
PRIMARY
EPA CompTox
DTXSID10453306
Created by admin on Mon Mar 31 22:24:51 GMT 2025 , Edited by admin on Mon Mar 31 22:24:51 GMT 2025
PRIMARY
FDA UNII
A7JNM906ZN
Created by admin on Mon Mar 31 22:24:51 GMT 2025 , Edited by admin on Mon Mar 31 22:24:51 GMT 2025
PRIMARY