137374-13-1

Usage

Purpose

Rodenticide for controlling rats and mice

Mechanism of action

Inhibits the activation of vitamin K, essential for blood clotting

Result of ingestion

Internal hemorrhaging and death in rodents

Form

Typically used in bait form

Classification

Anticoagulant rodenticide

Toxicity

Highly toxic to other animals, including pets and humans, if ingested

Regulation

Use is heavily regulated

Handling

Should only be handled by trained professionals

Upstream product

• 90466-78-7 5-acetoxyisophthalic acid 
• 618-83-7 5-Hydroxyisophthalic acid 

Downstream Products

• 252289-76-2 5-acetoxy-1,3-bis[N,N-bis(2-methoxyethyl)]benzenedicarboxamide 
• 224961-40-4 5-hydroxy-1,3-bis[N,N-bis(2-methoxyethyl)]benzenedicarboxamide 
• 252289-78-4 (3-[3-(3,5-bis-{[bis-(2-methoxy-ethyl)-amino]-methyl}-phenoxymethyl)-5-methylaminomethyl-benzyloxy]-5-{[bis-(2-methoxy-ethyl)-amino]-methyl}-benzyl)-bis-(2-methoxy-ethyl)-amine 
• 224961-41-5 3,5-bis-{3,5-bis-[bis-(2-methoxy-ethyl)-carbamoyl]-phenoxymethyl}-benzoic acid methyl ester 
• 252289-77-3 C₅₀H₇₃N₅O₁₅ 
• 1349701-96-7 3,5-bis(3-(3,4-bis(dodecyloxy)phenyl)-1,2,4-oxadiazol-5-yl)phenol 
• 1349701-92-3 C₇₂H₁₁₂N₄O₈ 
• 1349701-95-6 3,5-bis(3-(4-(dodecyloxy)phenyl)-1,2,4-oxadiazol-5-yl)phenol 
• 1349701-91-2 C₄₈H₆₄N₄O₆ 
• 1169389-59-6 3,5-bis(2-(4-tert-butylbenzoyl)hydrazinecarbonyl)phenyl acetate 

Relevant academic research and scientific papers

Columnar mesomorphism of bent-rod mesogens containing 1,2,4-oxadiazole rings

In this study, the synthesis, characterization, and mesomorphic properties of ten new bent-rod compounds containing two units of 1,2,4-oxadiazoles are reported. In order to understand the relationship between the structure and the mesomorphic behavior, molecules containing a variety of polar substituents (i.e., I, NO2, NH2, OH) on the central rigid core were prepared. The hexagonal columnar mesomorphism was characterized by DSC and POM and the nature of the mesophases was established through XRD studies. The driving force for self-assembly can be explained by microsegregation between the aliphatic parts and the polar parts, producing a dimer, trimer, and tetramer inside a single disc.

Dendrimers with alternating amine and ether generations

Dendrimers having alternating aryl benzyl ether and tertiary amine generations and up to 16 bis-(2-methoxyethyl)amine end groups and four internal tertiary amines were synthesized by sequential etherification, amidation of secondary amines, and LiAlH