32223-70-4

Usage

Uses

Used in Adhesives and Sealants Industry:
4-(Hexyloxy)phenyl isocyanate is used as a key component in the production of adhesives and sealants for its ability to enhance the bonding strength and durability of these products. Its presence in these formulations contributes to their effectiveness in various applications, such as construction, automotive, and packaging industries.
Used in Coatings Industry:
In the coatings industry, 4-(Hexyloxy)phenyl isocyanate is utilized as a critical ingredient in the formulation of coatings that offer improved adhesion, flexibility, and resistance to environmental factors. Its inclusion in coating formulations helps to achieve a longer-lasting and more robust protective layer on various substrates.
Used in Industrial Applications:
4-(Hexyloxy)phenyl isocyanate is used as a raw material in the synthesis of various chemical products and intermediates, which find applications in different industries. Its reactivity and versatility make it a valuable component in the development of new materials and compounds with specific properties tailored to meet industry needs.

InChI:InChI=1/C13H17NO2/c1-2-3-4-5-10-16-13-8-6-12(7-9-13)14-11-15/h6-9H,2-5,10H2,1H3

Upstream product

• 1142-39-8 para-hexyloxybenzoic acid 
• 32315-10-9 bis(trichloromethyl) carbonate 
• 39905-57-2 4-(n-hexyloxy)aniline 

Downstream Products

• 925597-38-2 1,3-bis(4-(hexyloxy)phenyl)urea 
• 1350641-65-4 benzene-1,3,5-tricarboxylic acid tris({3-[3-(4-hexyloxyphenyl)ureido]phenyl}amide) 
• 1350641-66-5 benzene-1,3,5-tricarboxylic acid tris({4-[3-(4-hexyloxyphenyl)ureido]phenyl}amide) 
• 561013-60-3 1-[4'-(2,4-dioxothiazolidin-5-ylmethyl)biphenyl-3-yl]-3-(4-hexyloxyphenyl)-1-methylurea 
• 112923-00-9 (4-Hexyloxy-phenyl)-carbamic acid 2-morpholin-4-yl-ethyl ester; hydrochloride 

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.

Using acetate anions to induce translational isomerization in a neutral urea-based molecular switch

Vying for urea: The translational isomerism of a neutral [2]rotaxane can be controlled in solution through the addition and removal of acetate anions. In the absence of acetate ions, the macrocyclic host recognizes a diphenylurea derivative; recognition of acetate ions by the urea-based station causes relocation of the macrocycle to another binding site (see picture). (Figure Presented).

Anthelmintic 1-(substituted phenyl)-3-alkanimidoyl ureas

The compounds of this invention are novel imidoylureas having anthelmintic activity and imidoylthioureas having antifertility activity. They are prepared by the reaction of appropriate amidines with appropriate isocyanates or isothiocyanates.