4460-02-0

Usage

Uses

Used in Medical/Surgical Applications:
Methyl 2,6-diisocyanatohexanoate is used as a component for creating synthetic adhesives and sealants due to its biocompatibility. This application is particularly relevant in the medical and surgical industries, where it can be utilized to bond tissues and seal wounds, promoting faster healing and reducing the risk of infection.
Used in the Chemical Industry:
In the chemical industry, Methyl 2,6-diisocyanatohexanoate is used as a versatile building block for the synthesis of various polymers and other compounds. Its unique chemical structure allows for the creation of materials with specific properties tailored to different applications, such as coatings, elastomers, and foams.
Used in Research and Development:
Methyl 2,6-diisocyanatohexanoate is also utilized in research and development settings, where it can be studied and modified to create new materials with improved properties. This can lead to the development of innovative products and technologies in various industries, including pharmaceuticals, materials science, and engineering.

InChI:InChI=1/C9H12N2O4/c1-15-9(14)8(11-7-13)4-2-3-5-10-6-12/h8H,2-5H2,1H3

Upstream product

• 590-28-3 potassium cyanate 
• 29547-05-5 2,6-Dibromhexansaeure-methylester 

Relevant academic research and scientific papers

ISOCYANATE PRODUCTION METHOD

An isocyanate production method according to the present invention is a method in which an isocyanate is produced by subjecting a carbamate to thermal decomposition, and includes: a step of preparing a mixture liquid containing the carbamate, an inactive solvent and a polyisocyanate compound; a step of conducting a thermal decomposition reaction of the carbamate by continuously introducing the mixture liquid into a thermal decomposition reactor; a step of collecting a low-boiling decomposition product by continuously extracting the low-boiling decomposition product in a gaseous state from the reactor, the low-boiling decomposition product having a boiling point lower than the polyisocyanate compound; and a step of collecting a high-boiling component by continuously extracting, from the reactor, a liquid phase component which is not collected in a gaseous state at the step of collecting the low-boiling decomposition product.

Aminosaeuren, I. Darstellung von Aminosaeuren aus Halogencarbonsaeure-alkylestern mit Alkalimetallcyanaten

α- and ω-halo- as well as α,ω-dihalocarboxylic alkyl esters react with potassium cyanate in the presence of alcohol at 80 - 120 deg C in dipolar aprotic solvents to yield α- and ω-(alkoxycarbonylamino)- and α,ω-bis(alkoxycarbonylamino)carboxylic alkyl esters, respectively, in good yields.Hydrolytic cleavage of these mono- or diurethanes with an aqueous solution of hydrochloric acid/formic acid leads to the corresponding amino acid hydrochlorides in nearly quantitative yields.