130224-95-2

Usage

Uses

Used in Materials Science and Chemistry:
BMBL is used as a monomer for the synthesis of advanced materials due to its high reactivity and ability to undergo polymerization reactions.
Used in UV-Curable Coatings:
BMBL is used as a crosslinking agent in the formulation of UV-curable coatings, enhancing their properties and performance.
Used in Bio-Based Materials Production:
BMBL is used in the production of bio-based materials, leveraging its biodegradability and biocompatibility.
Used in Biocompatible Polymers Development:
BMBL is used as a key component in the development of biocompatible polymers, contributing to their eco-friendly and safe characteristics for various applications.
Used in Drug Delivery Systems:
BMBL is utilized in the development of drug delivery systems, taking advantage of its biodegradability and biocompatibility to improve the efficacy and safety of drug administration.

InChI:InChI=1/C8H10O4/c1-5(2)8(10)12-6-3-7(9)11-4-6/h6H,1,3-4H2,2H3

Upstream product

• 5469-16-9 4-Hydroxy-dihydro-furan-2-on 
• 80-62-6 methacrylic acid methyl ester 
• 760-93-0 methacryloyl anhydride 
• 4245-37-8 vinyl methacrylate 
• 97-88-1 2-methyl-butyl acrylate 

Relevant academic research and scientific papers

METHOD FOR PRODUCING CARBOXYLIC ACID ESTER, ESTERIFICATION AGENT AND RING-OPENING ADDITION CATALYST

PROBLEM TO BE SOLVED: To provide a method for producing a carboxylic acid ester using a catalyst compound which is easy to handle and has high activity and to provide an esterification agent and a ring-opening addition catalyst suitably used for the production method. SOLUTION: An imidazole compound having a specific structure is allowed to exist during a reaction when a carboxylic acid ester is produced by reacting (A) at least one electrophilic body selected from the group consisting of at least one hydroxy group-donating compound selected from the group consisting of a phenol compound and alcohol and an epoxy group-donating compound composed of an epoxy compound and (B) at least one nucleophilic body selected from the group consisting of carboxylic acid, a carboxylic acid halide, a carboxylic acid ester and a carboxylic acid anhydride. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPO&INPIT

METHOD FOR MANUFACTRURING BETA-(METH)ACRYLOYLOXY-GAMMA-BUTYROLACTONES

The art relates to provision of a method for manufacturing an (meth)acrylic polymerizable monomer that can be used in various applications, such as an optical material, a resist material, a coating material and a laminate material, and provision of a new β-(meth)acryloyloxy-γ-butyrolactone compound by applying the manufacturing method. The method for manufacturing the β-(meth)acryloyloxy-γ-butyrolactone compound is described, in which a (meth)acrylate compound having a carbonyl group and a ketene compound are condensed and isomerized. Further, the manufacturing method is applied to the new β-(meth)acryloyloxy-γ-butyrolactone compound.

Process for producing monomer

A process for producing a monomer for resists represented by the following general formula 1: wherein R1 represents hydrogen or an optionally substituted alkyl group; R2, R3 and R4 each independently represent hydrogen or a substituent; and X, Y and Z each independently represent a direct bond or an optionally substituted alkylene group with 1 to 3 chain members, the process comprising carrying out esterification or transesterification in the presence of a biocatalyst.

PROCESS FOR PRODUCING LACTONE

A method for producing lactones, which comprises reacting an amide compound of Formula (I): [wherein X represents a halogen atom; R, R' and R1 to R6 each independently represents a hydrogen atom or any desired substituent; and n represents an integer of 0 to 2] with an aqueous medium.

Chemical amplifying type positive resist composition

A chemical amplifying type positive resist composition, excellent in balance of performance of resolution and sensitivity, having high dry etching resistance and comprising; a resin having a polymerization unit derived from a monomer represented by the following formula (I): wherein R1 and R2 independently represent hydrogen or an alkyl group having 1 to 4 carbons, and R3 represents hydrogen or a methyl group, the resin being insoluble in alkali itself but becoming alkali-soluble due to the action of an acid; and an acid generating agent is provided.

Process for preparing β-hydroxy-γ-butyrolactones and β-(meth)acryloyloxy-γ-butrolactones

The present invention provides a process for preparing β-hydroxy-γ-butyrolactone or β-methyl-β-hydroxy-γ-butyrolactone represented by the formula (1): wherein R1is hydrogen or methyl, which entails a) cyanating glycidol or 2-methyl-2,3-epoxypropanol, b) hydrolyzing the product of step a), and c) lactonizing the product of step b).