324787
2,2,2-Trifluoroethanesulfonyl chloride
99%
Synonym(s):
Tresyl chloride
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About This Item
Linear Formula:
CF3CH2SO2Cl
CAS Number:
Molecular Weight:
182.55
Beilstein:
1860983
EC Number:
MDL number:
UNSPSC Code:
12352101
PubChem Substance ID:
NACRES:
NA.22
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Assay
99%
form
liquid
refractive index
n20/D 1.388 (lit.)
bp
140-141 °C (lit.)
64-67 °C/45 mmHg (lit.)
density
1.651 g/mL at 25 °C (lit.)
functional group
fluoro
storage temp.
2-8°C
SMILES string
FC(F)(F)CS(Cl)(=O)=O
InChI
1S/C2H2ClF3O2S/c3-9(7,8)1-2(4,5)6/h1H2
InChI key
CXCHEKCRJQRVNG-UHFFFAOYSA-N
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accessory
Product No.
Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
161.6 °F - closed cup
Flash Point(C)
72 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Tohru Hayakawa et al.
Journal of biomedical materials research. Part A, 67(2), 684-688 (2003-10-21)
The aim of this study was to bind fibronectin directly to a titanium surface treated with tresyl chloride (2,2,2-trifluoroethanesulfonyl chloride) for the development of a strong connection of a dental implant to subepithelial connective tissues and/or peri-implant epithelia. Basic terminal
Tresyl chloride-activated supports for enzyme immobilization.
K Nilsson et al.
Methods in enzymology, 135, 65-78 (1987-01-01)
D A Puleo
Biomaterials, 17(2), 217-222 (1996-01-01)
Because of the limited mechanical properties of tissue substitutes formed by culturing cells on polymeric scaffolds, other approaches to tissue engineering must be explored for applications that require complete and immediate ability to bear weight, e.g. total joint replacements. Biochemical
Q Yang et al.
Analytical biochemistry, 268(2), 354-362 (1999-03-17)
For immobilized (proteo)liposome chromatography, unilamellar liposomes were covalently bound within gel beads that had been activated by CNBr, N-hydroxysuccinimide, tresyl, or chloroformate. Liposomes composed of phosphatidylcholine (PC) and 2 mol% of amino-containing lipid (phosphatidylethanolamine-caproylamine) were immobilized in the activated gels
Kristina Jonsson-Schmunk et al.
Drug metabolism and disposition: the biological fate of chemicals, 44(5), 758-770 (2016-02-13)
Landmark studies describing the effect of microbial infection on the expression and activity of hepatic CYP3A used bacterial lipopolysaccharide as a model antigen. Our efforts to determine whether these findings were translatable to viral infections led us to observations suggesting
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