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4-(BENZYLOXY)-2-METHYLPHENOL is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53325-49-8

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53325-49-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53325-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,2 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53325-49:
(7*5)+(6*3)+(5*3)+(4*2)+(3*5)+(2*4)+(1*9)=108
108 % 10 = 8
So 53325-49-8 is a valid CAS Registry Number.

53325-49-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-4-phenylmethoxyphenol

1.2 Other means of identification

Product number -
Other names 4-Benzyloxy-2-methyl-phenol

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:53325-49-8 SDS

53325-49-8Relevant academic research and scientific papers

PTERIDINES AND THEIR USE AS AGROCHEMICALS

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Page/Page column 30-31, (2011/04/14)

The present disclosure relates to 1- or 2-(4-(aryloxy)-phenyl)ethylamino-, oxy- or sulfanyl)pteridines and 1- or 2-(4-(heteroaryloxy)-phenyl)ethylamino-, oxy- or sulfanyl)pteridines and their use as agrochemicals and animal health products.

PTERIDINES AND THEIR USE AS AGROCHEMICALS

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Page/Page column 65, (2011/04/14)

The present disclosure relates to 1- or 2-(4-(aryloxy)-phenyl)ethylamino-, oxy- or sulfanyl)pteridines and 1- or 2-(4-(heteroaryloxy)-phenyl)ethylamino-, oxy- or sulfanyl)pteridines and their use as agrochemicals and animal health products.

OXAZOLE AND THIAZOLE PPAR MODULATORS

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Page/Page column 26, (2010/11/27)

The invention provides compounds (I) pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with the activity of the Peroxisome Proliferator-Activated Receptor (PPAR) families, particularly the activity of PPARδ.

COMPOUNDS AND COMPOSITIONS AS PPAR MODULATORS

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Page/Page column 58, (2008/06/13)

The invention provides compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with the activity of the Peroxisome Proliferator-Activated Receptor (PPAR) families.

COMPOUNDS AND COMPOSITIONS AS PPAR MODULATORS

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Page/Page column 45, (2010/11/27)

The invention provides compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with the activity of the Peroxisome Proliferator-Activated Receptor (PPAR) families.

An easy two-step reduction of salicylic acids and alcohols to 2-methylphenols

Mazzini, Francesco,Salvadori, Piero

, p. 2479 - 2481 (2007/10/03)

Salicylic acids and alcohols can be reduced to 2-methylphenols by a simple two steps procedure. Reaction conditions were optimized carrying out a study on the solvent effect and the amount of the reducing agent. The improved procedure resulted particularly useful in the synthesis of deuterated building blocks of biological interest. Georg Thieme Verlag Stuttgart.

Approaches to the preparation of 4-benzyloxy-2-(α,α,α- D3)methylphenol, a building block for labeled δ-tocopherol, and a new synthesis of R,R,R-5-D3-α-tocopherol

Mazzini, Francesco,Mandoli, Alessandro,Salvadori, Piero,Netscher, Thomas,Rosenau, Thomas

, p. 4864 - 4869 (2007/10/03)

Different routes are described for the synthesis of 4-benzyloxy-2-D 3-phenol, a key building block in the preparation of D 3-δ-tocopherol. Conditions for the improvement of Minami's reduction are also given, allowing a straightforward route to the title compound and a new synthesis of R,R,R-5-D3-α-tocopherol in good yields, starting from widely available R,R,R-α-tocopherol. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

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