52106-86-2

Basic information

• Product Name: Sodium 4-chloro-2-methylphenolate
• Synonyms: Sodium 4-chloro-2-methylphenolate
• CAS NO: 52106-86-2
• Molecular Formula: C₇H₆ClO*Na
• Molecular Weight: 165.57
• Mol File: 52106-86-2.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Sodium 4-chloro-2-methylphenolate(CAS DataBase Reference)
• NIST Chemistry Reference: Sodium 4-chloro-2-methylphenolate(52106-86-2)
• EPA Substance Registry System: Sodium 4-chloro-2-methylphenolate(52106-86-2)

Safety Data

• Hazardous Substances Data: 52106-86-2(Hazardous Substances Data)

Upstream product

• 1570-64-5 2-methyl-4-chlorophenol 

Downstream Products

• 42936-88-9 α-(2-methyl-4-chloro-phenoxy)-isobutyric acid 
• 93-65-2 (RS)-2-(4-chloro-o-tolyloxy)propionic acid 
• 115291-10-6 trichloro-methanesulfenic acid-(4-chloro-2-methyl-phenyl ester) 
• 105908-06-3 4-(4-chloro-2-methyl-phenoxy)-valeric acid 
• 25204-89-1 (4-chloro-2-methylphenoxy)butyric acid 
• 111049-01-5 diethyl-2-(2'-methyl-4-chloro-phenoxy)-propionyl-malonate 
• 23844-56-6 methyl R-2-(4-chloro-2-methylphenoxy)propanoate 
• 2401-55-0 C₃₂H₅₂Cl₂N₂O₂⁽²⁺⁾*2Br^(1-) 
• 63402-91-5 2-(4-Chloro-2-methyl-phenoxy)-3-methyl-butyric acid 3-phenoxy-benzyl ester 
• 63403-45-2 α(4-Chlor-2-methylphenoxy)-isovaleriansaeure 
• 83144-02-9 chloromethyl-(4-chloro-2-methyl-phenyl)-ether 
• 34645-94-8 [5-Chloro-2-(4-chloro-2-methyl-phenoxy)-phenyl]-acetic acid 
• 34645-98-2 [2-(4-Chloro-2-methyl-phenoxy)-5-methyl-phenyl]-acetic acid 
• 34645-90-4 [2-(4-Chloro-2-methyl-phenoxy)-phenyl]-acetic acid 

Relevant articles and documents

Method for synthesizing high-content 2-methyl-4-chloric acid and sodium salt

The invention discloses a method for synthesizing high-content 2-methyl-4-chloric acid and sodium salt. The method comprises the following steps: synthesizing 4-chloro-methylphenol from sulfuryl chloride by using a chlorination process, carrying out condensation with sodium chloroacetate, and drying filter cake, thereby obtaining sodium salt directly, or directly acidifying the filter cake, thereby obtaining 98% 2-methyl-4-chloric acid. Hydrochloric acid generated in the chlorination process can be recycled to an acidification procedure, and generated sulfur dioxide is further reacted with chlorine to prepare sulfuryl chloride which can be recycled for a chlorination procedure, so that a closed circulation green production process can be formed, and the product quality can be relatively greatly improved. According to the method, the cost is relatively low and the pollution is relatively slight, the equipment utilization rate is greatly increased, meanwhile the problem that the content is low if o-cresol is chloridized with chlorine can be solved, and a basis is made for producing 2-methyl-4-chloric acid through chlorination and condensation in sequence.