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36536-46-6

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36536-46-6 Usage

Description

(+/-)-B-BUTYROLACTONE, also known as gamma-butyrolactone (GBL), is a colorless, oily liquid with a slightly sweet taste. It is a chemical compound that has a wide range of industrial and commercial applications.
Used in Pharmaceutical Industry:
(+/-)-B-BUTYROLACTONE is used as a solvent for various pharmaceutical applications due to its ability to dissolve a wide range of substances.
Used in Agriculture Industry:
(+/-)-B-BUTYROLACTONE is used as a solvent in agriculture for its ability to dissolve various substances, making it useful in the production of certain agricultural chemicals.
Used in Electronics Industry:
(+/-)-B-BUTYROLACTONE is used as a solvent in the electronics industry for its ability to dissolve various substances, making it useful in the production of certain electronic components.
Used in Polymer Production:
(+/-)-B-BUTYROLACTONE is used as a precursor in the manufacturing of some polymers, contributing to the development of various plastic materials.
Used in Chemical Production:
(+/-)-B-BUTYROLACTONE is used as a precursor in the manufacturing of certain chemicals, playing a role in the production of specific chemical compounds.
Used as a Cleaning Agent:
(+/-)-B-BUTYROLACTONE is used as a cleaning agent due to its ability to dissolve various substances, making it effective for cleaning purposes.
Used in the Production of Gamma-Hydroxybutyrate (GHB):
(+/-)-B-BUTYROLACTONE has been used in the illegal production of the drug gamma-hydroxybutyrate (GHB), although its misuse and abuse have led to strict regulations and classification as a controlled substance in some countries.

Check Digit Verification of cas no

The CAS Registry Mumber 36536-46-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,5,3 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36536-46:
(7*3)+(6*6)+(5*5)+(4*3)+(3*6)+(2*4)+(1*6)=126
126 % 10 = 6
So 36536-46-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H6O2/c1-3-2-4(5)6-3/h3H,2H2,1H3

36536-46-6Relevant articles and documents

Carbonylative Polymerization of Epoxides Mediated by Tri-metallic Complexes: A Dual Catalysis Strategy for Synthesis of Biodegradable Polyhydroxyalkanoates

Li, Wen-Bing,Liu, Ye,Lu, Xiao-Bing,Yang, Jin-Chuang,Yang, Jun

supporting information, (2022/01/20)

Polyhydroxyalkanoates (PHAs) are a unique class of commercially manufactured biodegradable polyesters with properties suitable for partially substituting petroleum-based plastics. However, high costs and low volumes of production have restricted their application as commodity materials. In this study, tri-metallic complexes were developed for carbonylative polymerization via a dual catalysis strategy, and 17 products of novel PHAs with up to 38.2 kg mol?1 Mn values were discovered. The polymerization proceeds in a sequential fashion, which entails the carbonylative ring expansion of epoxide to β-lactone and its subsequent ring-opening polymerization that occurs selectively at the O-alkyl bond via carboxylate species. The wide availability and structural diversity of epoxide monomers provide PHAs with various structures, excellent functionalities, and tunable properties. This study represents a rare example of the preparation of PHAs using epoxides and carbon monoxide as raw materials.

Acrylonitrile Derivatives from Epoxide and Carbon Monoxide Reagents

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Paragraph 0223-0237, (2019/01/15)

The present invention is directed to reactor systems and processes for producing acrylonitrile and acrylonitrile derivatives. In preferred embodiments of the present invention, the processes comprise the following steps: introducing an epoxide reagent and carbon monoxide reagent to at least one reaction vessel through at least one feed stream inlet; contacting the epoxide reagent and carbon monoxide reagent with a carbonylation catalyst to produce a beta-lactone intermediate; polymerizing the beta-lactone intermediate with an initiator in the presence of a metal cation to produce a polylactone product; heating the polylactone product under thermolysis conditions to produce an organic acid product; optionally esterifying the organic acid product to produce one or more ester products; and reacting the organic acid product and/or ester product with an ammonia reagent under ammoxidation conditions to produce an acrylonitrile product.

Balancing between Heterogeneity and Reactivity in Porphyrin Chromium-Cobaltate Catalyzed Ring Expansion Carbonylation of Epoxide into β-Lactone

Rajendiran, Senkuttuvan,Ganesan, Vinothkumar,Yoon, Sungho

supporting information, p. 3283 - 3289 (2019/05/15)

The synthesis of a unique heterogeneous catalyst that combines the functionality of a homogeneous catalyst and the advantages of a heterogeneous catalytic process is a continuing goal in various industrially applicable reactions. Here, we report heterogenization of homogeneous catalyst for lactone production from epoxide carbonylation through a facile polymerization using Friedel-Crafts reaction. A correlation between reactivity and degree of heterogeneity has been deduced by synthesizing different sized polymeric catalysts. The partially polymerized catalyst showed a remarkable initial turnover frequency of 400 h-1, and the fully polymerized catalyst displayed excellent selectivity during recycling with a total turnover number of 4100.

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