5-(trifluoromethyl)thiophene-2-carboxylic acid

Synonym
Product Category
Product Code
CAS Number
MDL Number
Pubchem CID
Reaxys RN
5-(trifluoromethyl)-2-thenoic acid
Trifluoromethyl Building Blocks
KUMI3F105
128009-32-5
MFCD04421350
2049051
3542964
image-155171-Trimethyl(trifluoromethyl)silane_reagent.png
Chemical Name
Molecular Formula
Molecular Weight
Assay
Appearance
Melting Point
Packaging
Storage
5-(trifluoromethyl)thiophene-2-carboxylic acid
C6H3F3O2S
196.15
≥98%
Colorless to Off-white Solid
76-78°C
5g,10g,25g,50g,100g,250g and 500g
Store at room temperature
5-(trifluoromethyl)thiophene-2-carboxylic acid is an important building block for the synthesis of various trifluoromethyl-substituted organic compounds in pharmaceuticals, agrochemicals and material sciences, e.g. substituted 1,2,3-triazoles as NR2B receptor ligands for the treatment of disease states, disorders, and conditions mediated by NR2B receptor activity; positive allosteric modulators of α7 nAChRs for the treatment of disorders; Triazinone compound as T-type calcium channel inhibitor for the treatment of pain;Pesticidal pyrimidine in controlling pests such as insects and other invertebrates, etc..
Synthesis and polymerization of ethynylthiophenes and ethynylfurans containing trifluoromethyl groups. [1]
Reference:
[1] M.Nishida, et al, J. F. Chem., 1990, 46(3), pp 445-459.
Signal Word
Hazard Statements
Precautionary Statements
HS Code
RIDADR
Legal Information
Warning
H315,H319,H335
P264,P302+P352,P304+P340,P305+P351+P338

NONH for all modes of transport

1. Product Specification
2. Safety Data Sheet
Please inquire for pricing and availability of this product by writing email to sales@kumidas.com.