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3-Phenoxycycliccarbonate, also known as 3-phenoxy-1,2-epoxypropane, is an organic compound with the chemical formula C9H10O3. It is a colorless liquid that is soluble in organic solvents and has a molecular weight of 166.18 g/mol. 3-phenoxycycliccarbonate ;; is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential use as a reactive diluent in the production of epoxy resins, which are used in coatings, adhesives, and composite materials. Due to its reactivity, 3-phenoxycycliccarbonate requires careful handling and is typically stored under controlled conditions to prevent unwanted reactions.

4437-83-6

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4437-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4437-83-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,3 and 7 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4437-83:
(6*4)+(5*4)+(4*3)+(3*7)+(2*8)+(1*3)=96
96 % 10 = 6
So 4437-83-6 is a valid CAS Registry Number.

4437-83-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenyloxymethyl-[1,3]-dioxolan-2-one

1.2 Other means of identification

Product number -
Other names 4-phenyloxymethyl-1,3-dioxolan-2-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4437-83-6 SDS

4437-83-6Relevant academic research and scientific papers

Recyclable Bifunctional Polystyrene and Silica Gel-Supported Organocatalyst for the Coupling of CO2 with Epoxides

Kohrt, Christina,Werner, Thomas

, p. 2031 - 2034 (2015)

A bifunctional ammonium salt covalently bound to a polystyrene or silica support proved to be an efficient and recyclable catalyst for the solvent-free synthesis of cyclic carbonates from epoxides and CO2. The catalyst can be easily recovered b

The effective synthesis of propylene carbonate catalyzed by silica-supported hexaalkylguanidinium chloride

Xie, Haibo,Duan, Haifeng,Li, Shenghai,Zhang, Suobo

, p. 1199 - 1203 (2005)

We have described that both homogeneous and a silica-supported hexaalkylguanidinium chloride were effective catalysts for CO2 fixation to carbonate without any solvent under mild reaction conditions (4.5 MPa, 120 °C, 4 h), the silica-supported

Phenolic hydroxyl-functionalized imidazolium ionic liquids: Highly efficient catalysts for the fixation of CO2 to cyclic carbonates

Wu, Shi,Wang, Binshen,Zhang, Yongya,Elageed, Elnazeer H.M.,Wu, Haihong,Gao, Guohua

, p. 1 - 8 (2016)

A series of imidazolium ionic liquids were designed and synthesized by the reaction of imidazole derivatives with alkyl bromides. These ionic liquids were applied to catalyze the reaction of CO2 and epoxides. A detailed investigation was carried out on the relationship between catalytic activities and catalyst structures. The result showed that phenolic hydroxyl-functionalized imidazolium ionic liquids containing both phenolic hydroxyl and C2-H were highly efficient catalysts. Meanwhile, the spatial positions of the phenolic hydroxyl and C2-H in the imidazolium also exhibited great effect on the catalytic efficiencies, and the order of catalytic activity was meta-isomer > ortho-isomer > para-isomer. NMR titration and DFT calculations showed a synergetic effect, which C2-H and phenolic hydroxyl cooperatively activated epoxides by hydrogen bonds, was crucial for the reaction to proceed smoothly under mild conditions. In addition, the TOF of the most active catalyst 3-(3-phenolic hydroxyl)-1-butyl-imidazolium bromide (IL-2) reached to 900 h-1 in the reaction of CO2 and epichlorohydrin under the reaction conditions of 0.1 mol% catalyst, 1 MPa CO2, 120 °C and 1 h.

Cyclic carbonate synthesis from epoxides and CO2 over cyanocobalamin/n-Bu4NI

Bai, Dongsheng,Jing, Huanwang,Wang, Guangjian

, p. 600 - 603 (2012)

The synthesis of cyclic carbonates from epoxides and carbon dioxide catalyzed by cyanocobalamin and n-Bu4NI system was achieved under 0.8 MPa CO2 pressure at 140°C without organic solvents. Propylene carbonate was obtained in 99% yie

Cellulosic poly(ionic liquid)s: Synthesis, characterization and application in the cycloaddition of CO2 to epoxides

Chen, Qin,Peng, Chang,Xie, Haibo,Zhao, Zongbao Kent,Bao, Ming

, p. 44598 - 44603 (2015)

Cellulosic poly(ionic liquid)s (PILs) were prepared via nucleophilic substitution of chlorinated cellulose by 1-methyl-imidazole and their structure and thermal properties have been fully characterized; the cellulosic PILs were found to be green, efficien

Two Manganese Metalloporphyrin Frameworks Constructed from a Custom-Designed Porphyrin Ligand Exhibiting Selective Uptake of CO2over CH4and Catalytic Activity for CO2Fixation

Magnuson, Zachary L.,Cheng, Qigan,Zhang, Weijie,Chen, Yu-Sheng,Wojtas, Lukasz,Nafady, Ayman,Al-Enizi, Abdullah M.,Larsen, Randy W.,Zhang, X. Peter,Ma, Shengqian

, p. 2786 - 2792 (2021)

In this work, two new metal-metalloporphyrin frameworks (MMPFs), namely, MMPF-12 and MMPF-13, having unique structural formulas as [Mn24O78(Mn-dcdbp)12] and [Mn8.65(dcdbp)8](DMF)14(H2O)8, respectively, were synthesized via the reaction of the custom-desig

Efficient Conversion of Epoxides into Carbonates with CO 2 and a Single Organocatalyst: Laboratory and Kilogram-Scale Experiments

Azzouz, Rabah,Bischoff, Laurent,Contreras Moreno, Viviana,Derrouiche, Salim,Estel, Lionel,Herasme-Grullon, Clara,Ledoux, Alain,Levacher, Vincent,Marsais, Francis

, p. 183 - 188 (2020)

Cheap and readily available 2-aminopyridine and related compounds can be used as organocatalysts for the conversion of epoxides into cyclic carbonates. This reaction gives high conversions under solvent-free conditions and is amenable to a kilogram-scale

Functionalized zeolitic imidazolate framework F-ZIF-90 as efficient catalyst for the cycloaddition of carbon dioxide to allyl glycidyl ether

Jose, Tharun,Hwang, Yeseul,Kim, Dong-Woo,Kim, Moon-Il,Park, Dae-Won

, p. 61 - 67 (2015)

In this study, zeolitic imidazolate framework (ZIF-90) was synthesized from Zn(NO3)2·4H2O and imidazolate-2-carboxyaldehyde (ICA), then it was post-functionalized to form F-ZIF-90 using hydrazine followed by quaternization

Porous Metal-Organic Frameworks with Chelating Multiamine Sites for Selective Adsorption and Chemical Conversion of Carbon Dioxide

Zhao, Dan,Liu, Xiao-Hui,Guo, Jin-Han,Xu, Hua-Jin,Zhao, Yue,Lu, Yi,Sun, Wei-Yin

, p. 2695 - 2704 (2018)

A combination of carbon dioxide (CO2) capture and chemical fixation in a one-step process is attractive for chemists and environmentalists. In this work, by incorporating chelating multiamine sites to enhance the binding affinity toward CO

Amino-functional imidazolium ionic liquids for CO2 activation and conversion to form cyclic carbonate

Yue, Chengtao,Su, Dan,Zhang, Xu,Wu, Wei,Xiao, Linfei

, p. 1313 - 1321 (2014)

A series of amino-functional imidazolium ionic liquids have been prepared and used as catalysts for cycloaddition of CO2 with epoxide. The reactions generated the cyclic carbonate even at room temperature under atmospheric pressure. Under the o

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