28439-86-3

Usage

Uses

Used in the Polyurethane Industry:
4-N-Butoxyphenyl isocyanate is used as a key intermediate in the production of polyurethane materials for its ability to react and form stable polymers. It contributes to the creation of flexible and rigid foams, which are essential in various applications such as insulation, cushioning, and packaging.
Used in the Coatings Industry:
In the coatings sector, 4-N-Butoxyphenyl isocyanate serves as a critical component in formulating durable and high-performance coatings. Its reactivity allows for the development of coatings with enhanced properties such as abrasion resistance, chemical resistance, and adhesion.
Safety Considerations:
Due to its potential to cause skin and respiratory irritation, 4-N-butoxyphenyl isocyanate should be handled with care. It is imperative to use appropriate personal protective equipment (PPE) to minimize exposure risks during its production, transportation, and application processes.

InChI:InChI=1/C11H13NO2/c1-2-3-8-14-11-6-4-10(5-7-11)12-9-13/h4-7H,2-3,8H2,1H3

Upstream product

• 75-44-5 phosgene 
• 4344-55-2 para-butoxyaniline 
• 32315-10-9 bis(trichloromethyl) carbonate 
• 1498-96-0 4-butoxybenzoic acid 

Downstream Products

• 96062-93-0 (4-butoxy-phenyl)-carbamic acid-(2-hydroxy-3-piperidino-propyl ester) 
• 115915-66-7 1,2-bis-(4-butoxy-phenylcarbamoyloxy)-3-piperidino-propane 
• 38145-73-2 3-(4-Butoxy-phenyl)-1-{[(E)-4-chloro-2-methyl-phenylimino]-methyl}-1-methyl-urea 
• 112922-94-8 (4-Butoxy-phenyl)-carbamic acid 2-morpholin-4-yl-ethyl ester; hydrochloride 
• 117221-96-2 N-(4-butoxyphenyl)-N'-[5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl]urea 
• 105126-46-3 5-Nitro-indazole-1-carboxylic acid (4-butoxy-phenyl)-amide 
• 86764-39-8 1,1-Dibenzyl-3-(4-butoxy-phenyl)-urea 
• 895638-52-5 C₁₁H₁₆N₂O₃ 
• 1119859-55-0 3-amino-N-(4-butoxyphenyl)-1H-indazole-1-carboxamide 
• 1119859-86-7 N-(4-butoxyphenyl)-3-(([(4-butoxyphenyl)amino]carbonyl)amino)-1H-indazole-1-carboxamide 
• 1252574-61-0 N-(4-butoxyphenyl)-N'-{2-[(7-chloroquinolin-4-yl)amino]-ethyl}urea 
• 1621608-39-6 N-(4-butoxyphenyl)-2-{[4-(tricyclo[3.3.1.1^3,7]dec-1-yl)quinolin-2-yl]carbonyl}hydrazinecarboxamide 

Relevant academic research and scientific papers

Oxime Carbamate-Discovery of a series of novel FAAH inhibitors

A series of novel oxime carbamates have been identified as potent inhibitors of the key regulatory enzyme of the endocannabinoid signaling system, fatty acid amide hydrolase (FAAH). In this Letter, the rationale behind the discovery and the biological evaluations of this novel class of FAAH inhibitors are presented. Both in vitro and in vivo results of selected targets are discussed, along with inhibition kinetics and molecular modeling studies.1.

Quantitative Structure-Activity Relationships of Insecticidal Pyrazolines

Methyl 3-(4-chlorophenyl)-4-methyl-1--2-pyrazoline-4-carboxylates and related compounds were prepared. Their convulsant activity was determined as the minimum dose required to bring about the symptom within 1 h after injection against male adult American cockroaches, Periplaneta americana (L.). Insecticidal activity with metabolic inhibitors for oxidation and hydrolysis was measured 24 h after injection of the test compounds. Variations in each of the activities were analysed by using physicochemical substituent parameters and regression analysis. The findings indicated that the greater the hydrophobicity and the more the electron-withdrawing property of the substituents, the higher were the activities. Variations in each of the two activities were parabolically related to the STERIMOL width parameter with an optimum value of about zero.