Description

(6,8-Dichloro-3-Ethyl-4-Oxo-3,4-Dihydro-Quinazolin-2-Ylsulfanyl)-Acetic Acid is a high-purity, synthetic organic compound belonging to the quinazolinone class, serving as a critical pharmaceutical intermediate and research chemical. Its unique molecular structure, featuring a dichloro-substituted quinazolinone core linked to an acetic acid moiety via a sulfanyl bridge, makes it a valuable building block for medicinal chemistry and advanced material science. This compound is primarily sought by R&D laboratories and manufacturers in the pharmaceutical and agrochemical sectors for developing novel active ingredients.

Application

• Pharmaceutical Intermediate: Key precursor in the synthesis of novel drug candidates, particularly those targeting kinase inhibition or possessing antimicrobial properties.
• Medicinal Chemistry Research: Used as a scaffold or building block for structure-activity relationship (SAR) studies and library synthesis in drug discovery programs.
• Agrochemical Development: Serves as an intermediate in the research and production of new-generation herbicides or fungicides.
• Chemical Biology Probes: Utilized in the development of molecular probes for studying enzyme function and biological pathways.
• Organic Synthesis: Acts as a versatile reagent for constructing complex heterocyclic systems in academic and industrial research settings.

Basic Information

Product Name	(6,8-Dichloro-3-Ethyl-4-Oxo-3,4-Dihydro-Quinazolin-2-Ylsulfanyl)-Acetic Acid
CAS No.	886500-42-1
Molecular Formula	C₁₂H₁₀Cl₂N₂O₃S
Molecular Weight	333.19 g/mol
Synonyms	2-[(6,8-Dichloro-3-ethyl-4-oxo-3,4-dihydroquinazolin-2-yl)thio]acetic acid; (6,8-Dichloro-3-ethyl-4-oxo-3,4-dihydroquinazolin-2-yl)sulfanylacetic acid; 2-((6,8-Dichloro-3-ethyl-4-oxo-3,4-dihydroquinazolin-2-yl)thio)acetic acid; Quinazolin-2-ylthioacetic acid derivative; CAS 886500-42-1
EINECS	Contact for details

Quality Control

Our (6,8-Dichloro-3-Ethyl-4-Oxo-3,4-Dihydro-Quinazolin-2-Ylsulfanyl)-Acetic Acid is manufactured under a strict quality management system. Every batch undergoes comprehensive analytical testing to ensure high purity and consistent composition, meeting the rigorous standards required for pharmaceutical R&D. A detailed Certificate of Analysis (COA) providing purity, identity, and impurity profile is supplied with each shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at room temperature (15-25°C). Keep away from incompatible materials. Due to its light-sensitive nature, handling should be conducted under appropriate conditions to maintain product integrity.

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%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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