Description

4,6-Dimethoxy-n-[4-(Trifluoromethyl)Phenyl]-5-Pyrimidinesulfonamide is a high-purity, advanced pharmaceutical intermediate and research chemical. This compound is valued for its role as a key building block in the synthesis of complex molecules, particularly in medicinal chemistry and agrochemical development. It is essential for researchers and manufacturers in the pharmaceutical, agrochemical, and fine chemical industries seeking to develop novel active ingredients.

Application

• Pharmaceutical Intermediate: A critical precursor in the synthesis of active pharmaceutical ingredients (APIs), particularly for candidates targeting various disease pathways.
• Agrochemical Research: Serves as a key scaffold for developing new herbicides, fungicides, and insecticides, leveraging the pyrimidine and sulfonamide moieties.
• Medicinal Chemistry: Used in drug discovery programs for structure-activity relationship (SAR) studies and lead optimization.
• Fine Chemical Synthesis: Employed in custom synthesis and the production of specialized, high-value chemical compounds.
• Biochemical Research: May be utilized as a tool compound or inhibitor in biochemical assays and proteomics research.

Basic Information

Product Name	4,6-Dimethoxy-n-[4-(Trifluoromethyl)Phenyl]-5-Pyrimidinesulfonamide
CAS No.	861208-73-3
Molecular Formula	C13H12F3N3O4S
Molecular Weight	363.31 g/mol
Synonyms	4,6-Dimethoxy-N-[4-(trifluoromethyl)phenyl]pyrimidine-5-sulfonamide; 5-Pyrimidinesulfonamide, 4,6-dimethoxy-N-[4-(trifluoromethyl)phenyl]-; N-(4-Trifluoromethylphenyl)-4,6-dimethoxypyrimidine-5-sulfonamide; 4,6-Dimethoxy-5-[[[4-(trifluoromethyl)phenyl]amino]sulfonyl]pyrimidine
EINECS	Contact for details

Quality Control

Our 4,6-Dimethoxy-n-[4-(Trifluoromethyl)Phenyl]-5-Pyrimidinesulfonamide is manufactured under strict quality management systems. Every batch undergoes rigorous analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. A comprehensive Certificate of Analysis (COA) is provided with each shipment, detailing all specifications and test results. We support compliance with cGMP and ICH guidelines for pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). The product should be kept under an inert atmosphere if long-term stability is required. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Water Content (KF)	≤ 0.5%
Residue on Ignition	≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.