6430-91-7

Usage

Appearance

White to off-white crystalline powder

Usage

Primarily in veterinary medicine

Purpose

Anticoccidial agent for prevention and treatment of coccidiosis in poultry, particularly broiler chickens

Mechanism of Action

Inhibits development and proliferation of coccidian parasites

Administration

Typically administered orally

Effectiveness

Effective against multiple species of coccidia

Safety

Low toxicity, considered safe for use in food-producing animals when used according to proper dosage and administration guidelines

Upstream product

• 102-47-6 3,4-Dichlorophenylmethyl chloride 
• 75-16-1 methylmagnesium bromide 
• 6725-44-6 methyl 2-(3,4-dichlorophenyl)acetate 
• 5807-30-7 3,4-dichlorophenyl acetic acid 

Downstream Products

• 83149-58-0 2-Amino-propionic acid 2-(3,4-dichloro-phenyl)-1,1-dimethyl-ethyl ester 

Relevant academic research and scientific papers

Copper-Catalyzed and Indium-Mediated Methoxycarbonylation of Unactivated Alkyl Iodides with Balloon CO

This work emphasizes the synthesis of alkyl esters via Cu-catalyzed and In-mediated alkoxycarbonylation of unactivated alkyl iodides in the presence of In or InI. The reactions were suitable for the preparation of primary, secondary, and even tertiary alkyl esters, representing an exceptionally rare example for the creation of quaternary carbon centers upon formation of esters. The preliminary mechanistic studies indicated that alkyl radicals were involved, and Cu/In/CO played a cooperative role in the carbonylation event.

Synergistic Catalysis for the Umpolung Trifluoromethylthiolation of Tertiary Ethers

The first transition-metal-free, site-specific umpolung trifluoromethylthiolation of tertiary alkyl ethers has been developed, achieving the challenging tertiary C(sp3)–SCF3 coupling under redox-neutral conditions. The synergism of organophotocatalyst 4CzIPN and BINOL-based phosphorothiols can site-selectively cleave tertiary sp3 C(sp3)–O ether bonds in complex molecules initiated by a polarity-matching hydrogen-atom-transfer (HAT) event. The incorporation of several competing benzylic and methine C(sp3)?H bonds in alkyl ethers has little influence on the regioselectivity. Selective difluoromethylthiolation of C?O bonds has also been achieved. This represents not only an important step forward in trifluoromethylthiolation but also a promising means for site-selective C?O bond functionalization of unsymmetrical tertiary alkyl ethers.

2-METHYL-1-(SUBSTITUTED)PHENYL-2-PROPYL ESTERS OF 2-AMINOPROPANOIC ACID

A compound of the general formula and pharmaceutically acceptable salts thereof, in which formula the groups R0 are the same or different and are selected from the group consisting of hydrogen, halogen, alkyl having 1, 2 or 3 carbon atoms, and alkoxy having 1, 2 or 3 carbon atoms; R1 is hydrogen, methyl or ethyl; R2 is methyl or ethyl; R3 and R4 are the same or different and are hydrogen or an alkyl group having 1, 2 or 3 carbon atoms; and n is 0, 1 or 2. Pharmaceutical preparations containing these compounds are useful for treatment of depressive disorders