Home Sulfos Ytterbium(iii) trifluoromethanesulfonate

Ytterbium(iii) trifluoromethanesulfonate

CAS No.:
54761-04-5
Catalog Number:
AG00DBGQ
Molecular Formula:
C3F9O9S3Yb
Molecular Weight:
620.2613
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
99%
In Stock USA
United States
$39
- +
5g
97%
In Stock USA
United States
$40
- +
25g
97%
In Stock USA
United States
$144
- +
100g
97%
In Stock USA
United States
$413
- +
Product Description
Catalog Number:
AG00DBGQ
Chemical Name:
Ytterbium(iii) trifluoromethanesulfonate
CAS Number:
54761-04-5
Molecular Formula:
C3F9O9S3Yb
Molecular Weight:
620.2613
MDL Number:
MFCD06200261
IUPAC Name:
trifluoromethanesulfonate;ytterbium(3+)
InChI:
InChI=1S/3CHF3O3S.Yb/c3*2-1(3,4)8(5,6)7;/h3*(H,5,6,7);/q;;;+3/p-3
InChI Key:
AHZJKOKFZJYCLG-UHFFFAOYSA-K
SMILES:
FC(S(=O)(=O)[O-])(F)F.FC(S(=O)(=O)[O-])(F)F.FC(S(=O)(=O)[O-])(F)F.[Yb+3]
UNII:
4N70OSW24G
Properties
Complexity:
145  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
4  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
620.795g/mol
Formal Charge:
0
Heavy Atom Count:
25  
Hydrogen Bond Acceptor Count:
18  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
620.244g/mol
Monoisotopic Mass:
620.795g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
197A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Literature
Title Journal
Efficient synthesis of isochromanones and isoquinolines via Yb(OTf)3-catalyzed tandem oxirane/aziridine ring opening/Friedel-Crafts cyclization. Chemical communications (Cambridge, England) 20120307
Acid-responsive microcapsules: the loading-unloading processes. Chemical communications (Cambridge, England) 20111121
Layer-by-layer assembly and electrochemical study of a 4-aminothiophenol and ytterbium(III) trifluoromethanesulfonate hydrate film on a gold electrode. The Analyst 20111007
Yb(OTf)3 catalyzed new cascade reaction: a facile assembly of fused quinazolinones. Chemical communications (Cambridge, England) 20111007
Formal [4 + 2] cycloaddition of alkoxy-substituted donor-acceptor cyclobutanes and aldehydes catalyzed by Yb(OTf)3. Organic letters 20101105
Ytterbium triflate catalyzed synthesis of alkoxy-substituted donor-acceptor cyclobutanes and their formal [4 + 2] cycloaddition with imines: stereoselective synthesis of piperidines. Organic letters 20101105
Self-assembled organic-inorganic hybrid silica with ionic liquid framework: a novel support for the catalytic enantioselective Strecker reaction of imines using Yb(OTf)(3)-pybox catalyst. Chemical communications (Cambridge, England) 20101007
Synthesis of procyanidin B3 and its anti-inflammatory activity. the effect of 4-alkoxy group of catechin electrophile in the Yb(OTf)(3)-catalyzed condensation with catechin nucleophile. The Journal of organic chemistry 20100716
Selective approach toward multifunctionalized lactams by lewis acid promoted PhSe group transfer radical cyclization. The Journal of organic chemistry 20100521
Yb(OTf)3-catalyzed construction of indole derivatives through formal [3+3] cycloaddition of 1,1-vinylidenecyclopropanediesters with nitrones. Chemistry (Weinheim an der Bergstrasse, Germany) 20100125
Catalytic asymmetric Strecker hydrocyanation of imines using Yb(OTf)3-pybox catalysts. Chemical communications (Cambridge, England) 20090914
Ytterbium(III) triflate-catalyzed amination of 1-cyclopropylprop-2-yn-1-ols as an expedient route to conjugated enynes. The Journal of organic chemistry 20090220
Efficient chemical synthesis of a dodecasaccharidyl lipomannan component of mycobacterial lipoarabinomannan. The Journal of organic chemistry 20081219
A study on the synthesis of calix[4 and 6]arenes using alternately arranged phloroglucinols and p-tert-butylphenols. Chemical & pharmaceutical bulletin 20080801
Synthesis of 1,2,4-triazole C-nucleosides from hydrazonyl chlorides and nitriles. Nucleosides, nucleotides & nucleic acids 20070101
Properties