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2417-10-9

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2417-10-9 Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 47, p. 509, 2004 DOI: 10.1021/jm030182iTetrahedron Letters, 36, p. 7363, 1995 DOI: 10.1016/0040-4039(95)01657-0

Check Digit Verification of cas no

The CAS Registry Mumber 2417-10-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,1 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2417-10:
(6*2)+(5*4)+(4*1)+(3*7)+(2*1)+(1*0)=59
59 % 10 = 9
So 2417-10-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H10O2/c13-11-8-4-5-9-12(11)14-10-6-2-1-3-7-10/h1-9,13H

2417-10-9SDS

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 2-phenoxyphenol

1.2 Other means of identification

Product number -
Other names o-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:2417-10-9 SDS

2417-10-9Relevant articles and documents

Degradation of the antibacterial agents triclosan and chlorophene using hydrodechlorination by Al-based alloys

Pérko, Jan,Kamenická, Barbora,Weidlich, Tomá?

, p. 1777 - 1786 (2018)

Abstract: Triclosan and chlorophene are chlorinated phenols used as antimicrobial agents. Both compounds are ordinarily detected in aquatic environments. The aim of this study is to prove the reactivity of three different metallic alloys used as common re

Iron-catalyzed arene C-H hydroxylation

Cheng, Lu,Wang, Huihui,Cai, Hengrui,Zhang, Jie,Gong, Xu,Han, Wei

, p. 77 - 81 (2021/10/05)

The sustainable, undirected, and selective catalytic hydroxylation of arenes remains an ongoing research challenge because of the relative inertness of aryl carbon-hydrogen bonds, the higher reactivity of the phenolic products leading to over-oxidized by-products, and the frequently insufficient regioselectivity. We report that iron coordinated by a bioinspired L-cystine-derived ligand can catalyze undirected arene carbon-hydrogen hydroxylation with hydrogen peroxide as the terminal oxidant. The reaction is distinguished by its broad substrate scope, excellent selectivity, and good yields, and it showcases compatibility with oxidation-sensitive functional groups, such as alcohols, polyphenols, aldehydes, and even a boronic acid. This method is well suited for the synthesis of polyphenols through multiple carbon-hydrogen hydroxylations, as well as the late-stage functionalization of natural products and drug molecules.

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.].

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