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713-68-8

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713-68-8 Usage

Chemical Properties

CLEAR PALE YELLOW LIQUID

General Description

The thermodynamic properties of 3-phenoxyphenol was studied using a combination of effusion and calorimetric techniques and also by high-level ab initio molecular orbital calculations. The standard molar enthalpy of formation of 3-phenoxyphenol was determined using Calvet microcalorimetry.

Check Digit Verification of cas no

The CAS Registry Mumber 713-68-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,1 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 713-68:
(5*7)+(4*1)+(3*3)+(2*6)+(1*8)=68
68 % 10 = 8
So 713-68-8 is a valid CAS Registry Number.
InChI:InChI=1/C12H10O2/c13-10-5-4-8-12(9-10)14-11-6-2-1-3-7-11/h1-9,13H

713-68-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenoxyphenol

1.2 Other means of identification

Product number -
Other names meta-phenoxyphenol

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:713-68-8 SDS

713-68-8Relevant articles and documents

Synthesis and properties of 2,3,9,10,16,17,23,24-octakis(3-phenoxyphenoxy)phthalocyanine and its complexes with erbium of diverse structures

Koptyaev,Ageeva,Galanin,Shaposhnikov

, p. 261 - 267 (2016)

Reaction of 4,5-dichlorophthalonitrile with 3-phenoxyphenol led to the formation of 4,5-bis(3-phenoxyphenoxy)phthalonitrile. It has underlain the synthesis of 2,3,9,10,16,17,23,24-octakis(3-phenoxy-phenoxy) phthalocyanine and its single and double deck sandwich complexes with erbium. As show the electron absorption spectra the complexes are dissociated in dichloromethane at concentrations below 1 × 10-5 mol L-1.

CoII Immobilized on Aminated Magnetic-Based Metal–Organic Framework: An Efficient Heterogeneous Nanostructured Catalyst for the C–O Cross-Coupling Reaction in Solvent-Free Conditions

Mohammadinezhad, Arezou,Akhlaghinia, Batool

, p. 332 - 352 (2020/01/11)

Abstract: In this paper, we report the synthesis of Fe3O4?AMCA-MIL53(Al)-NH2-CoII NPs based on the metal–organic framework structures as a magnetically separable and environmentally friendly heterogeneous nanocatalyst. The prepared nanostructured catalyst efficiently promotes the C–O cross-coupling reaction in solvent-free conditions without the need for using toxic solvents and/or expensive palladium catalyst. Graphic Abstract: [Figure not available: see fulltext.].

A catalytic oxidation fragrant boron class compound preparing phenol method (by machine translation)

-

Paragraph 0027; 0043; 0044, (2017/08/08)

The invention discloses a method for catalytic oxidation of phenolic compounds fragrant boron class compound synthesis method, the flux in the solvent in the aqueous solution, under the action of alkali, adding hydrazine hydrate or acid hydrazides catalyst, catalytic oxidation fragrant boron class compound directly for the preparation of phenolic compound. The invention of the method of preparation of the phenol compound, the catalyst is a cheap hydrazine hydrate or hydrazine compound, the oxidizing agent is atmospheric pressure of air or oxygen, the reaction does not need good and activeness metal catalyst, is extensive and stable substrate, substrate-sensitive functional group compatibility good and wide range of application. In the optimized under the reaction conditions, the yield of the target product separation up to 99%. (by machine translation)

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