40590-38-3

Basic information

• Product Name: Phenol, 3,4-dimethyl-, potassium salt
• CAS NO: 40590-38-3
• Molecular Formula: C8H10O.K
• Molecular Weight: 160.257
• Mol File: 40590-38-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Phenol, 3,4-dimethyl-, potassium salt(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 3,4-dimethyl-, potassium salt(40590-38-3)
• EPA Substance Registry System: Phenol, 3,4-dimethyl-, potassium salt(40590-38-3)

Safety Data

• Hazardous Substances Data: 40590-38-3(Hazardous Substances Data)

Upstream product

• 95-65-8 3,4-Dimethylphenol 

Downstream Products

• 138827-21-1 Cu(3,4-dimethylphenoxo)2(2,2'-bipyridine) 
• 937598-95-3 4-(3,4-dimethylphenoxy)benzylamine 
• 85958-26-5 Potassium; 4-(3,4-dimethyl-phenoxy)-2-[(furan-2-ylmethyl)-amino]-5-sulfamoyl-benzenesulfonate 
• 344881-94-3 4-(3,4-Dimethyl-phenoxy)-2-[(furan-2-ylmethyl)-amino]-5-sulfamoyl-benzenesulfonic acid phenyl ester 
• 100763-50-6 N⁴-Benzyl-6-(3,4-dimethyl-phenoxy)-pyrimidine-2,4-diamine 
• 25141-00-8 2-(3,4-dimethyl-phenoxy)-propionic acid 
• 153472-91-4 2-(3,4-dimethyl-phenoxy)-propionic acid ethyl ester 
• 100763-74-4 2-amino-4-(3,4-xylyloxy)-6-chloropyrimidine 

Relevant articles and documents

Design, synthesis, insecticidal, and acaricidal activities of novel pyrimidinamine derivatives containing a biphenyl ether

A series of original pyrimidinamine derivatives containing a biphenyl ether moiety were designed and synthesized. Their structures were confirmed by 1H NMR, MS, and elemental analyses. Their insecticidal activities against lepidopteran and hemiptera insects and acaricidal activities were tested. The results of bioassay demonstrated that 9k showed the best activity (LC50 = 2.08 mg/L) against Tetranychus urticae, which is comparable with the positive control, spirotetramat (LC50 = 2.27 mg/L), and 9g showed better activity (LC50 = 0.52 mg/L) against Aphis fabae than the positive control, imidacloprid (LC50 = 1.02 mg/L), and relatively good activity (LC50 = 2.49 mg/L) against T urticae. Their structure-activity relationships indicated that both an ethyl group on the 4-position of the pyrimidine ring and alkyl chain as a para-substituent group of the benzene ring showed good biological activity.