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1,2-Propanediol, 3,3'-[1,3-phenylenebis(oxy)]bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

7324-53-0

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7324-53-0 Usage

Type

Organic compound

Uses

Solvent, moisturizer in cosmetic and pharmaceutical products, food additive, production of polyester resins, antifreeze, and de-icing solutions

Toxicity

Relatively non-toxic and safe for human use

Importance

Widely utilized ingredient in various consumer products

Check Digit Verification of cas no

The CAS Registry Mumber 7324-53-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,2 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7324-53:
(6*7)+(5*3)+(4*2)+(3*4)+(2*5)+(1*3)=90
90 % 10 = 0
So 7324-53-0 is a valid CAS Registry Number.

7324-53-0SDS

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 3-[3-(2,3-dihydroxypropoxy)phenoxy]propane-1,2-diol

1.2 Other means of identification

Product number -
Other names 1,2-Propanediol,3,3'-[1,3-phenylenebis(oxy)]bis

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:7324-53-0 SDS

7324-53-0Downstream Products

7324-53-0Relevant academic research and scientific papers

MnIII Porphyrins: Catalytic Coupling of Epoxides with CO2 under Mild Conditions and Mechanistic Considerations

Milani, Jorge L. S.,Meireles, Alexandre M.,Bezerra, Werberson A.,Martins, Dayse. C. S.,Cangussu, Danielle,das Chagas, Rafael P.

, p. 4393 - 4402 (2019)

A series of 5,10,15,20-tetrakis(2,3-dichlorophenyl)porphyrinate complexes of manganese(III) [MnIII(T2,3DCPP)X] with six different axial ligands (X=NO3 ?, AcO?, IO3 ?, Br?, Cl?, HO?) were investigated as catalysts in the cycloaddition reactions of CO2 and styrene oxide (SO), under mild conditions, i. e., atmospheric pressure and 60 °C. [MnIIIT(2,3DCPP)IO3] showed the best catalytic performance, selectively producing the respective cyclic carbonate from diverse epoxides using tetrabutylammonium bromide as a nucleophile source. Mechanistic considerations were inferred from electronic spectra and spectrophotometric titrations, showing that there are a series of equilibriums involved in the formation of the catalytic active species. Stability constants for the proposed equilibrium models were determined using SQUAD software. A catalytic cycle has been proposed based on those observations.

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