6274-27-7

Basic information

• Product Name: 2,5-DICHLOROPHENYLTHIOGLYCOLIC ACID
• Synonyms: ((2,5-dichlorophenyl)thio)-aceticaci;((2,5-dichlorophenyl)thio)aceticacid;[(2,5-dichlorophenyl)thio]-aceticaci;2,5-dichlorophenylthioglycolacid;2,5-DICHLOROPHENYLTHIOGLYCOLIC ACID;Dichlorophenylthioglycolicacid;2-(2,5-dichlorophenylthio)acetic acid;NSC 36971
• CAS NO: 6274-27-7
• Molecular Formula: C₈H₆Cl₂O₂S
• Molecular Weight: 237.1
• EINECS: 228-468-3
• Mol File: 6274-27-7.mol
• Article Data: 2

Chemical Properties

• Melting Point: 129°C
• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• Solubility: soluble in Alcohol
• CAS DataBase Reference: 2,5-DICHLOROPHENYLTHIOGLYCOLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-DICHLOROPHENYLTHIOGLYCOLIC ACID(6274-27-7)
• EPA Substance Registry System: 2,5-DICHLOROPHENYLTHIOGLYCOLIC ACID(6274-27-7)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• RTECS: AG9041000
• Hazardous Substances Data: 6274-27-7(Hazardous Substances Data)

Usage

General Description

2,5-Dichlorophenylthioglycolic acid is a chemical compound that is primarily used as a herbicide and plant growth regulator. It belongs to the class of thiocarboxylic acids and is known for its ability to inhibit the growth of plants by interfering with their hormone regulation. 2,5-DICHLOROPHENYLTHIOGLYCOLIC ACID is often used in agriculture to control the growth of undesirable plants and weeds. It works by disrupting the synthesis of auxin, a plant hormone that is essential for the regulation of plant growth. In addition to its agricultural uses, 2,5-dichlorophenylthioglycolic acid is also used in research and industrial applications. However, it is important to handle this chemical with caution as it may have adverse effects on human health and the environment.

Upstream product

• 5858-18-4 2,5-dichlorbenzenethiol 
• 79-11-8 chloroacetic acid 
• 5402-73-3 2,5-dichlorobenzenesulphonyl chloride 
• 106-46-7 para-dichlorobenzene 
• 33663-41-1 2,5-dichloroaniline hydrochloride 
• 68-11-1 mercaptoacetic acid 
• 79-08-3 bromoacetic acid 

Downstream Products

• 115893-61-3 (2,5-dichloro-phenylsulfanyl)-acetic acid amide 
• 14295-43-3 4,7,4',7'-tetrachloro-[2,2']bi[benzo[b]thiophenylidene]-3,3'-dione 
• 105892-15-7 (2,5-Dichloro-phenylsulfanyl)-acetic acid; compound with 2-[bis-(2-hydroxy-ethyl)-amino]-ethanol 
• 181375-13-3 (6-R-trans)-3-(chloromethyl)-7-[[[(2,5-dichlorophenyl)thio]acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid, diphenylmethyl ester 
• 1370637-75-4 C₃₀H₂₅Cl₃N₂O₆S 

Relevant articles and documents

Synthesis and anti-MRSA activity of novel cephalosporin derivatives

Cephalosporin derivatives containing a unique combination of lipophilic C-7 sidechains and polar C-3 thiopyridinium groups were synthesized and found to exhibit potent anti-MRSA activity in vitro and in vivo. The optimum C-7 sidechains utilized were 2,5-dichlorophenylthioacetamido and 2,6-dichloropyrid-4-ylthioacetamido. The C-3 thiopyridinium rings were substituted at nitrogen with amino acid and pyruvic acid groups that were designed to confer aqueous solubility as required for IV formulation. This paper describes the characteristics of these novel cephalosporins and highlights synthetic methods developed to allow their practical, large-scale syntheses. (C) 2000 Elsevier Science Ltd.