T27006
2-Thenoyltrifluoroacetone
99%
Synonym(s):
4,4,4-Trifluoro-1-(2-thienyl)-1,3-butanedione, TTA (extractant), TTB, TTFA
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C8H5F3O2S
CAS Number:
Molecular Weight:
222.18
Beilstein:
168645
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.
Recommended Products
Quality Level
Assay
99%
bp
96-98 °C/8 mmHg (lit.)
mp
40-44 °C (lit.)
storage temp.
2-8°C
SMILES string
FC(F)(F)C(=O)CC(=O)c1cccs1
InChI
1S/C8H5F3O2S/c9-8(10,11)7(13)4-5(12)6-2-1-3-14-6/h1-3H,4H2
InChI key
TXBBUSUXYMIVOS-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Application
Reagent for the determination of actinides and lanthanides.[1]
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
233.6 °F - closed cup
Flash Point(C)
112 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Vladimir A Kokorekin et al.
Molecules (Basel, Switzerland), 25(18) (2020-09-17)
In this article, we demonstrate how an original effective "metal-free" and "chromatography-free" route for the synthesis of 3-thiocyanatopyrazolo[1,5-a]pyrimidines has been developed. It is based on electrooxidative (anodic) C-H thiocyanation of 5-aminopyrazoles by thiocyanate ion leading to 4-thiocyanato-5-aminopyrazoles (stage 1, yields
Jeffery, G.H. et al.
Vogel's Textbook of Quantitative Chemical Analysis, 170-170 (1989)
Tao Huang et al.
Journal of cellular biochemistry, 107(5), 973-983 (2009-06-06)
Gap junctional intercellular communication (GJIC) plays a critical role in the control of multiple cell behavior as well as in the maintenance of tissue and organ homeostasis. However, mechanisms involved in the regulation of gap junctions (GJs) have not been
David González-Aragón et al.
Biochemical pharmacology, 73(3), 427-439 (2006-11-25)
Dicoumarol, a competitive inhibitor of NAD(P)H:quinone oxidoreductase 1 (NQO1), increases intracellular superoxide and affects cell growth of tumor cells. This work was set to establish a mechanistic link between dicoumarol, superoxide and cell cycle alterations in HL-60 cells. Using ES936
A Lemarie et al.
Cell death and differentiation, 18(2), 338-349 (2010-08-14)
The formation of reactive oxygen species (ROS) and the change of the intracellular pH (pH(i)) are common phenomena during apoptosis. How they are interconnected, however, is poorly understood. Here we show that numerous anticancer drugs and cytokines such as Fas
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
