Home Sulfos Trifluoromethanesulfonamide

Trifluoromethanesulfonamide

CAS No.:
421-85-2
Catalog Number:
AG003V2G
Molecular Formula:
CH2F3NO2S
Molecular Weight:
149.0923
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
97%
In Stock USA
United States
$19
- +
5g
97%
In Stock USA
United States
$50
- +
10g
97%
In Stock USA
United States
$88
- +
25g
97%
In Stock USA
United States
$207
- +
100g
97%
In Stock USA
United States
$613
- +
Product Description
Catalog Number:
AG003V2G
Chemical Name:
Trifluoromethanesulfonamide
CAS Number:
421-85-2
Molecular Formula:
CH2F3NO2S
Molecular Weight:
149.0923
MDL Number:
MFCD00068714
IUPAC Name:
trifluoromethanesulfonamide
InChI:
InChI=1S/CH2F3NO2S/c2-1(3,4)8(5,6)7/h(H2,5,6,7)
InChI Key:
KAKQVSNHTBLJCH-UHFFFAOYSA-N
SMILES:
FC(S(=O)(=O)N)(F)F
Properties
Complexity:
161  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
148.976g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
149.087g/mol
Monoisotopic Mass:
148.976g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
68.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.1  
Literature
Title Journal
Cyclooxygenase-1-selective inhibitors based on the (E)-2'-des-methyl-sulindac sulfide scaffold. Journal of medicinal chemistry 20120308
Bis(tetra-phenyl-phospho-nium) bis-[N-(trifluoro-methyl-sulfon-yl)dithio-carbimato(2-)-κS,S']zincate(II). Acta crystallographica. Section E, Structure reports online 20120101
Discovery of new chromone containing sulfonamides as potent inhibitors of bovine cytosolic carbonic anhydrase. Bioorganic & medicinal chemistry 20110601
Synthesis of N-[2-(2,4-Difluorophenoxy)trifluoromethyl-3-pyridyl]sulfonamides and their inhibitory activities against secretory phospholipase A₂. Chemical & pharmaceutical bulletin 20110101
4-[N-(substituted 4-pyrimidinyl)amino]benzenesulfonamides as inhibitors of carbonic anhydrase isozymes I, II, VII, and XIII. Bioorganic & medicinal chemistry 20101101
Synthesis and investigation of inhibition effect of fluorinated sulfonamide derivatives on carbonic anhydrase. European journal of medicinal chemistry 20100301
Versatile Pd(OTf)2 x 2 H2O-catalyzed ortho-fluorination using NMP as a promoter. Journal of the American Chemical Society 20090610
Titration calorimetry standards and the precision of isothermal titration calorimetry data. International journal of molecular sciences 20090601
Automated potentiometric titrations in KCl/water-saturated octanol: method for quantifying factors influencing ion-pair partitioning. Analytical chemistry 20090401
Design, synthesis and evaluation of trifluoromethane sulfonamide derivatives as new potent and selective peroxisome proliferator-activated receptor alpha agonists. Bioorganic & medicinal chemistry letters 20080115
Development of efficient Lewis acid catalysts for intramolecular cycloaddition reactions of ester-tethered substrates. Chemical record (New York, N.Y.) 20070101
LiTFSI structure and transport in ethylene carbonate from molecular dynamics simulations. The journal of physical chemistry. B 20060316
New metabolically stabilized analogues of lysophosphatidic acid: agonists, antagonists and enzyme inhibitors. Biochemical Society transactions 20051201
Direct, facile aldehyde and ketone alpha-selenenylation reactions promoted by L-prolinamide and pyrrolidine sulfonamide organocatalysts. The Journal of organic chemistry 20050708
Design, synthesis, and pharmacological evaluation of pyridinic analogues of nimesulide as cyclooxygenase-2 selective inhibitors. Journal of medicinal chemistry 20041230
The synthesis and structure-activity relationships of 3-amino-4-benzylquinolin-2-ones; discovery of novel KCNQ2 channel openers. Bioorganic & medicinal chemistry letters 20040405
Variations of acidic functions at position 2 and substituents at positions 4, 5 and 6 of the indole moiety and their effect on NMDA-glycine site affinity. European journal of medicinal chemistry 20031001
Structure-based design and discovery of novel inhibitors of protein tyrosine phosphatases. Bioorganic & medicinal chemistry 20030417
Synthesis and structural comparison of triaryl(sulfonylimino)pnictoranes. Inorganic chemistry 20020408
Properties