Welcome to LookChem.com Sign In|Join Free

CAS

  • or

623-53-0

Post Buying Request

623-53-0 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

623-53-0 Usage

Uses

Different sources of media describe the Uses of 623-53-0 differently. You can refer to the following data:
1. Non-aqueous solvent for Li-ion batteries
2. Alkyl carbonates find applications as solvents for lithium ion battery electrolytes and the use of high quality battery grade electrolytes having extremely low water (<10 ppm) and acid (<10 ppm) contents are critical for achieving high electrochemical performance.
3. EMC is majorly utilized as a co-solvent in the nonaqueous electrolyte. It enhances the energy density and discharge capacity of lithium-ion batteries.

General Description

This product has been enhanced for energy efficiency.

Check Digit Verification of cas no

The CAS Registry Mumber 623-53-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,2 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 623-53:
(5*6)+(4*2)+(3*3)+(2*5)+(1*3)=60
60 % 10 = 0
So 623-53-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H8O3/c1-3-7-4(5)6-2/h3H2,1-2H3

623-53-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (754935)  Ethyl methyl carbonate Green Alternative  99%

  • 623-53-0

  • 754935-50ML

  • 1,722.24CNY

  • Detail
  • Aldrich

  • (809934)  Ethyl methyl carbonate  99.9%, acid <10 ppm, H2O <10ppm

  • 623-53-0

  • 809934-25G

  • 2,533.05CNY

  • Detail
  • Aldrich

  • (752002)  Ethyl methyl carbonate  98%

  • 623-53-0

  • 752002-10ML

  • 483.21CNY

  • Detail
  • Aldrich

  • (752002)  Ethyl methyl carbonate  98%

  • 623-53-0

  • 752002-50ML

  • 1,714.05CNY

  • Detail
  • Aldrich

  • (752002)  Ethyl methyl carbonate  98%

  • 623-53-0

  • 752002-100ML

  • 3,092.31CNY

  • Detail

623-53-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl Methyl Carbonate

1.2 Other means of identification

Product number -
Other names Ethyl methyl carbonate

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:623-53-0 SDS

623-53-0Synthetic route

ethanol
64-17-5

ethanol

methyl chloroformate
79-22-1

methyl chloroformate

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

Conditions
ConditionsYield
With 1,2-dimethyl-1H-imidazole at 0 - 20℃; for 1h; Product distribution / selectivity;98.1%
With 1-methyl-1H-imidazole at 0 - 20℃; for 1h;97.4%
With 1-methyl-1H-imidazole In bis-2-propyl carbonate at 0 - 20℃; for 1h;97.6%
ethanol
64-17-5

ethanol

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

Conditions
ConditionsYield
With dicobalt octacarbonyl at 180℃; for 1h; chemoselective reaction;98%
With Novozyme 435 at 60℃; for 24h; Green chemistry; Enzymatic reaction;90.3%
With lanthanum(III) chloride; calcium chloride; sodium hydroxide at 90℃; for 12h; Reagent/catalyst; Molecular sieve; Glovebox;51.47%
3-Methyl-4-phenyl-4H-pyridine-1-carboxylic acid ethyl ester
132819-56-8

3-Methyl-4-phenyl-4H-pyridine-1-carboxylic acid ethyl ester

A

3-methyl-4-phenyl-pyridine
2052-92-8

3-methyl-4-phenyl-pyridine

B

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

Conditions
ConditionsYield
With sodium methylate In methanol at 18℃; anodic oxidation (graphite-rod electrodes), 6 F/mol passed through the solution;A 90%
B n/a
carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

Diethyl carbonate
105-58-8

Diethyl carbonate

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

Conditions
ConditionsYield
With Zeolitic imidazole framework (ZIF)-67 at 100℃; for 24h; Reagent/catalyst; Concentration;83.39%
With Mg/Fe oxide calcined at 400°C at 100℃; for 1.5h; Catalytic behavior; Reagent/catalyst; Temperature;66%
With Zn(2-methylimidazolate)2 at 100℃; for 3h; Reagent/catalyst; Temperature; Time;65.7%
ethanol
64-17-5

ethanol

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

A

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

B

Diethyl carbonate
105-58-8

Diethyl carbonate

Conditions
ConditionsYield
With sodium methylate In methanol at 69 - 120℃; for 6h; Reflux;A n/a
B 73%
With silica-alumina at 78℃; under 760.051 Torr; for 2h; pH=11; Reagent/catalyst; Temperature;A 63.9%
B n/a
With 15percentMgO-5percentMgCl-2percentLa2CO3 supported on Al2O3-SiO2 at 200℃; under 760.051 Torr; Reagent/catalyst; Temperature;A 57.37%
B n/a
ethanol
64-17-5

ethanol

methyl N-hydroxycarbamate
584-07-6

methyl N-hydroxycarbamate

A

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

B

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

Conditions
ConditionsYield
With lead dioxide In dichloromethane at 40℃; for 0.166667h;A 14.3%
B 70%
With lead dioxide at 40℃; for 0.166667h; Product distribution; reaction at -10 deg C; other alcohols, water; oxidation of alkyl N-hydroxycarbamates in the presence of alcohols; competitive alcoholysis; effect of the nature of alkyl group, alcohol reactivity, temperature on the product ratio;A 14.3%
B 70%
methanol
67-56-1

methanol

ethyl N-hydroxylcarbamate
589-41-3

ethyl N-hydroxylcarbamate

A

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

B

Diethyl carbonate
105-58-8

Diethyl carbonate

Conditions
ConditionsYield
With lead dioxide In dichloromethane at 40℃; for 0.166667h;A 25.1%
B 66.3%
1-ethoxycarbonyl-4-phenyl-1,4-dihydropyridine
82126-20-3

1-ethoxycarbonyl-4-phenyl-1,4-dihydropyridine

A

p-phenylpyridine
939-23-1

p-phenylpyridine

B

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

Conditions
ConditionsYield
With sodium methylate In methanol at 18℃; anodic oxidation (graphite-rod electrodes), 6 F/mol passed through the solution;A 65%
B n/a
2-Methyl-4-phenyl-4H-pyridine-1-carboxylic acid ethyl ester
132819-55-7

2-Methyl-4-phenyl-4H-pyridine-1-carboxylic acid ethyl ester

A

2-methyl-4-phenylpyridine
15032-21-0

2-methyl-4-phenylpyridine

B

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

Conditions
ConditionsYield
With sodium methylate In methanol at 18℃; anodic oxidation (graphite-rod electrodes);A 60%
B n/a
diethyl dibromomalonate
631-22-1

diethyl dibromomalonate

cyclohexene
110-83-8

cyclohexene

A

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

B

7,7-dibromonorcarane
2415-79-4

7,7-dibromonorcarane

Conditions
ConditionsYield
With sodium methylate at 0℃;A n/a
B 60%
With sodium methylate at 0℃; Mechanism; reactions under var. conditions;A n/a
B 60%
ethanol
64-17-5

ethanol

carbon dioxide
124-38-9

carbon dioxide

methyl iodide
74-88-4

methyl iodide

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

Conditions
ConditionsYield
Stage #1: carbon dioxide With 1-butyl-3-methyl-1H-imidazol-3-iumhydrogencarbonate at 25℃; under 760.051 Torr; for 6h;
Stage #2: ethanol; methyl iodide at 25℃; under 760.051 Torr; for 12h;
57.6%
ethyl acetate
141-78-6

ethyl acetate

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

A

acetic acid methyl ester
79-20-9

acetic acid methyl ester

B

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

C

Diethyl carbonate
105-58-8

Diethyl carbonate

Conditions
ConditionsYield
lithium methanolate at 77℃; for 3h; Product distribution / selectivity;A n/a
B 50%
C n/a
lithium amide at 78℃; for 4h; Product distribution / selectivity;A n/a
B 50%
C n/a
lithium methanolate at 78℃; for 3h; Product distribution / selectivity;A n/a
B 50%
C n/a
lithium amide at 77℃; for 4h; Product distribution / selectivity;A n/a
B 47%
C n/a
acetic acid methyl ester
79-20-9

acetic acid methyl ester

Diethyl carbonate
105-58-8

Diethyl carbonate

A

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

B

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

Conditions
ConditionsYield
lithium methanolate at 78℃; for 3h; Product distribution / selectivity;A 50%
B n/a
methanol
67-56-1

methanol

ethyl N-acetoxy-N-methoxycarbamate
745829-72-5

ethyl N-acetoxy-N-methoxycarbamate

A

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

B

N-Ethoxycarbonyl-O-methylhydroxylamine
3871-28-1

N-Ethoxycarbonyl-O-methylhydroxylamine

C

ethyl N,N-dimethoxycarbamate

ethyl N,N-dimethoxycarbamate

Conditions
ConditionsYield
at 20℃; for 98h;A 44.4%
B 7.3%
C 33.9%
methanol
67-56-1

methanol

ethyl N-acetoxy-N-isopropoxycarbamate

ethyl N-acetoxy-N-isopropoxycarbamate

A

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

B

ethyl N-isopropoxy-N-isopropoxycarbamate

ethyl N-isopropoxy-N-isopropoxycarbamate

Conditions
ConditionsYield
at 20℃; for 120h;A 38.7%
B 44%
ethanol
64-17-5

ethanol

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

A

methanol
67-56-1

methanol

B

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

C

Diethyl carbonate
105-58-8

Diethyl carbonate

Conditions
ConditionsYield
lithium methanolate at 78℃; for 4h; Product distribution / selectivity;A n/a
B 44%
C n/a
4-methyl-2-phenyl-2H-pyridine-1-carboxylic acid ethyl ester
63755-37-3

4-methyl-2-phenyl-2H-pyridine-1-carboxylic acid ethyl ester

A

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

B

4-methyl-2-phenylpyridine
3475-21-6

4-methyl-2-phenylpyridine

Conditions
ConditionsYield
With sodium methylate In methanol at 18℃; anodic oxidation (graphite-rod electrodes);A n/a
B 38%
trimethyl orthoformate
149-73-5

trimethyl orthoformate

ethyl N-chloro-N-methoxycarbamate
745829-70-3

ethyl N-chloro-N-methoxycarbamate

A

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

B

N-Ethoxycarbonyl-O-methylhydroxylamine
3871-28-1

N-Ethoxycarbonyl-O-methylhydroxylamine

Conditions
ConditionsYield
In methanol at -8 - 5℃; for 21h;A 22%
B 35%
2-Butyl-4-methyl-2H-pyridine-1-carboxylic acid ethyl ester
132819-57-9

2-Butyl-4-methyl-2H-pyridine-1-carboxylic acid ethyl ester

A

2-n-butyl-4-methylpyridine
6304-31-0

2-n-butyl-4-methylpyridine

B

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

Conditions
ConditionsYield
With sodium methylate In methanol at 18℃; anodic oxidation (graphite-rod electrodes);A 31%
B n/a
methanol
67-56-1

methanol

ethyl N-chloro-N-methoxycarbamate
745829-70-3

ethyl N-chloro-N-methoxycarbamate

A

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

B

N-Ethoxycarbonyl-O-methylhydroxylamine
3871-28-1

N-Ethoxycarbonyl-O-methylhydroxylamine

C

N,N'-bis(ethoxycarbonyl)-N,N'-dimethoxyhydrazine
90222-29-0

N,N'-bis(ethoxycarbonyl)-N,N'-dimethoxyhydrazine

Conditions
ConditionsYield
With sodium acetate at 30 - 31℃; for 96h;A 30%
B 11%
C 14%
methanol
67-56-1

methanol

ethanol
64-17-5

ethanol

carbon dioxide
124-38-9

carbon dioxide

A

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

B

carbonic acid dimethyl ester
616-38-6

carbonic acid dimethyl ester

C

Diethyl carbonate
105-58-8

Diethyl carbonate

Conditions
ConditionsYield
titanium tetramethoxide at -168 - 150℃; for 15h; Cooling with ethanol-dry ice;A 23%
B 2%
C 3%
methanol
67-56-1

methanol

(ethoxydichloromethyl)sulfenyl chloride
87463-09-0

(ethoxydichloromethyl)sulfenyl chloride

A

methylene chloride
74-87-3

methylene chloride

B

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

methanol
67-56-1

methanol

chloroformic acid ethyl ester
541-41-3

chloroformic acid ethyl ester

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

sodium methylate
124-41-4

sodium methylate

chloroformic acid ethyl ester
541-41-3

chloroformic acid ethyl ester

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

sodium ethanolate
141-52-6

sodium ethanolate

methyl chloroformate
79-22-1

methyl chloroformate

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

methanol
67-56-1

methanol

trans-N.N'-Dinitroso-N.N'-dicarbethoxy-1.4-diamino-cyclohexan
100314-09-8

trans-N.N'-Dinitroso-N.N'-dicarbethoxy-1.4-diamino-cyclohexan

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

Conditions
ConditionsYield
With sodium methylate In cyclohexanone
ethanol
64-17-5

ethanol

1-Methoxycarbonyl-3,5-dimethyl-pyridinium; chloride
107820-42-8

1-Methoxycarbonyl-3,5-dimethyl-pyridinium; chloride

A

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

B

3,5-dimethyl-pyridinium-chloride
36316-70-8

3,5-dimethyl-pyridinium-chloride

Conditions
ConditionsYield
at 25℃; Thermodynamic data; ΔH(excit.), ΔS(excit.);
ethanol
64-17-5

ethanol

3-Cyano-1-methoxycarbonyl-pyridinium; chloride

3-Cyano-1-methoxycarbonyl-pyridinium; chloride

A

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

B

3-cyanopyridine hydrochloride
65520-09-4

3-cyanopyridine hydrochloride

Conditions
ConditionsYield
at 25℃; Mechanism; Thermodynamic data; other 1-methoxycarbonylpyridinium chlorides; ΔH(excit.), ΔS(excit.);
diethyl dicarbonate
1609-47-8

diethyl dicarbonate

dimethyl dicarbonate
4525-33-1

dimethyl dicarbonate

A

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

B

carbon dioxide
124-38-9

carbon dioxide

Conditions
ConditionsYield
In dichloromethane Ambient temperature;
2,2-Dichloro-3,3-diethoxy-propionic acid ethyl ester
160663-37-6

2,2-Dichloro-3,3-diethoxy-propionic acid ethyl ester

sodium methylate
124-41-4

sodium methylate

A

dichloroacetaldehyde diethyl acetal
619-33-0

dichloroacetaldehyde diethyl acetal

B

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

Conditions
ConditionsYield
In diethyl ether at 20℃; for 4h;
ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

boron trifluoride
7637-07-2

boron trifluoride

BF3-EMC
220991-85-5

BF3-EMC

Conditions
ConditionsYield
for 48h; Schlenk technique; Inert atmosphere; Glovebox;97%
2,2,2-trifluoroethanol
75-89-8

2,2,2-trifluoroethanol

ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

methyl (2,2,2-trifluoroethyl) carbonate

methyl (2,2,2-trifluoroethyl) carbonate

Conditions
ConditionsYield
With tributylmethylammonium bis(trifluoromethanesulfonyl)imide salt In triethylamine at 50 - 80℃; for 15h; Temperature; Autoclave; Large scale;91%
ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

1-(4-methoxyphenyl)ethanone
100-06-1

1-(4-methoxyphenyl)ethanone

ethyl 4-methoxybenzoylacetate
2881-83-6

ethyl 4-methoxybenzoylacetate

Conditions
ConditionsYield
Stage #1: ethyl methyl carbonate With sodium hydride at 20℃; Inert atmosphere;
Stage #2: 1-(4-methoxyphenyl)ethanone for 4h; Inert atmosphere; Reflux;
86%
ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

para-methylacetophenone
122-00-9

para-methylacetophenone

ethyl (4-methylbenzoyl)acetate
27835-00-3

ethyl (4-methylbenzoyl)acetate

Conditions
ConditionsYield
Stage #1: ethyl methyl carbonate With sodium hydride at 20℃; Inert atmosphere;
Stage #2: para-methylacetophenone for 4h; Inert atmosphere; Reflux;
83%
ethyl methyl carbonate
623-53-0

ethyl methyl carbonate

para-bromoacetophenone
99-90-1

para-bromoacetophenone

ethyl 4-Bromobenzoylacetate
26510-95-2

ethyl 4-Bromobenzoylacetate

Conditions
ConditionsYield
Stage #1: ethyl methyl carbonate With sodium hydride at 20℃; Inert atmosphere;
Stage #2: para-bromoacetophenone for 4h; Inert atmosphere; Reflux;
80%

623-53-0Relevant articles and documents

Zeolitic imidazolate framework as efficient heterogeneous catalyst for the synthesis of ethyl methyl carbonate

Zhou, Xi,Zhang, Hong Ping,Wang, Gong Ying,Yao, Zhi Gang,Tang, Ying Ran,Zheng, Shan Shan

, p. 43 - 47 (2013)

A zeolitic imidazolate framework (ZIF-8) was developed as a novel efficient heterogeneous catalyst for the synthesis of ethyl methyl carbonate from dimethyl carbonate and diethyl carbonate. ZIF-8 was characterized by element analysis, X-ray powder diffraction (XRD), Fourier transform infrared (FT-IR), temperature programmed desorption (TPD), N2 adsorption-desorption and thermogravimetric analysis. The effects of catalyst amount, temperature and reaction time on the yield of ethyl methyl carbonate were also tested. The results showed that ZIF-8 performed excellent activity, selectivity and reusability under mild reaction conditions.

Amorphous mesoporous aluminophosphate as highly efficient heterogeneous catalysts for transesterification of diethyl carbonate with dimethyl carbonate

Shi, Jinghui,Liu, Gang,Fan, Zhiqiang,Nie, Liying,Zhang, Zhihui,Zhang, Wenxiang,Huo, Qisheng,Yan, Wenfu,Jia, Mingjun

, p. 721 - 725 (2011)

The catalytic performance of an amorphous mesoporous aluminophosphate (AlPO) was investigated for the transesterification of diethyl carbonate (DEC) with dimethyl carbonate (DMC) to synthesize ethyl methyl carbonate (EMC). Compared with other solid acid a

Zeolitic imidazole framework-67 as an efficient heterogeneous catalyst for the synthesis of ethyl methyl carbonate

Yang, Lili,Yu, Lin,Sun, Ming,Gao, Cheng

, p. 86 - 90 (2014)

Zeolitic imidazole framework (ZIF)-67, a novel environmentally benign catalyst, was developed for the preparation of ethyl methyl carbonate (EMC) from dimethyl carbonate and diethyl carbonate. EMC was obtained in 83.39% yield using ZIF-67 as the catalyst when compared to that obtained using ZIF-8 catalyst. NH3 and CO2 temperature-programmed desorption methods were used to evaluate the presence of both acidic and basic sites in ZIF-67 catalyst. The lager surface area of ZIF-67 favors for the adsorption of reactants over the solid surface of the catalyst, facilitating the formation of EMC. Moreover, ZIF-67 catalyst exhibited excellent reusability without significant loss in its catalytic activity.

Mg and Al dual-metal functionalized mesoporous carbon as highly efficient heterogeneous catalysts for the synthesis of ethyl methyl carbonate

Cui, Yunzuo,Hao, Xiyun,Lin, Yanan,Liu, Chunling,Shi, Jinghui,Wang, He,Xue, Xiangxin,Zhang, Zhihui

, p. 21199 - 21205 (2021/12/09)

Mg and Al dual-metal functionalized nanoscale porous carbon materials (MgAl@NC) with highly ordered mesoporous structures and mixed active sites were successfully prepared using a simple one-pot synthesis method. The catalytic properties of the resultant MgAl@NC catalysts were investigated for the synthesis of ethyl methyl carbonate (EMC) in a fixed bed reactor. The catalysts exhibited remarkably high activity, selectivity and stability for the transesterification of diethyl carbonates (DEC) with dimethyl carbonates (DMC) even under high LHSV conditions. A 50.0% DEC conversion and a 99.2% EMC selectivity could be obtained at 103 °C and an LHSV = 7.8 h-1. The catalyst maintained a high product yield with almost no decrease in catalytic performance after 360 h. The well-dispersed magnesium aluminate spinel and α-cristobalite formed neighboring acid-base sites, while the synergistic catalytic effects of the mixed active sites should be critical for activation of the reactants. It may also be the reason for the efficient production of EMC under very high LHSV conditions.

Method for synthesizing organic carbonate from carbon dioxide, alcohol and brominated alkane under mild conditions

-

Paragraph 0016-0017; 0021, (2020/06/02)

The invention discloses a method for synthesizing organic carbonate from carbon dioxide, alcohol and brominated alkane under mild conditions, belonging to the field of chemical synthesis. According tothe method, carbon dioxide, alcohol and brominated alkane are used as raw materials, 1,8-diazabicycloundec-7-ene (DBU) is used as an activating agent, and acetonitrile is used as a solvent to preparethe organic carbonate. The target product, namely the organic carbonate with excellent yield can be obtained under optimized reaction conditions. The method is mild in reaction conditions, simple andconvenient to operate and high in yield, and is an excellent system for preparing the organic carbonate.

Improved Synthesis of Unsymmetrical Carbonate Derivatives Using Calcium Salts

Hamada, Tomohito,Okada, Michiaki,Yamauchi, Akiyoshi,Kishikawa, Yosuke

, p. 667 - 673 (2019/04/25)

An effective synthetic method for unsymmetrical carbonate species has been developed. Calcium oxide and calcium hydroxide were found to be highly effective for this reaction, affording unsymmetrical carbonates in high yield and purity. Calcium chloride, which is a coproduct, serves as a water scavenger that can be easily removed. Additional drying processes and complicated purification steps are not necessary in this reaction. This improved process is important in terms of green sustainable chemistry principles.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 623-53-0