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Phenol, 2-ethoxy-6-methyl-, also known as 6-Methyl-2-ethoxyphenol or 2-Ethoxy-6-methylphenol, is an organic compound with the chemical formula C9H12O2. It is a derivative of phenol, featuring a methyl group at the 6th carbon and an ethoxy group at the 2nd carbon. This colorless to pale yellow liquid is soluble in water and has a distinct phenolic odor. It is primarily used as an intermediate in the synthesis of various chemicals, including pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactivity and functional groups, it can undergo a range of chemical reactions, making it a versatile building block in organic chemistry.

2563-06-6

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2563-06-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2563-06-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2563-06:
(6*2)+(5*5)+(4*6)+(3*3)+(2*0)+(1*6)=76
76 % 10 = 6
So 2563-06-6 is a valid CAS Registry Number.

2563-06-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethoxy-6-methylphenol

1.2 Other means of identification

Product number -
Other names Phenol,2-ethoxy-6-methyl

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:2563-06-6 SDS

2563-06-6Relevant academic research and scientific papers

Facile and regioselective dealkylation of alkyl aryl ethers using niobium(V) pentachloride

Sudo, Yukinori,Arai, Shigeru,Nishida, Atsushi

, p. 752 - 758 (2007/10/03)

A simple and facile method for the cleavage of carbon-oxygen bonds promoted by niobium pentachloride(V) is described. Excellent yields and regioselectivities were observed with various alkyl aryl ethers to give the phenols. NMR studies revealed the formation of monoaryloxy niobium salt(V), and a neighboring-group effect may play a significant role in the regioselectivity. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.

A simple and regioselective carbon-oxygen bond cleavage using Niobium(V)

Arai, Shigeru,Sudo, Yukinori,Nishida, Atsushi

, p. 1104 - 1106 (2007/10/03)

A simple and convenient method for the differentiation of alkoxy groups on aromatic rings is described. Niobium(V) is found to possess a strong Lewis acid property to transform alkyl arylethers smoothly to the corresponding phenols in high yields. The excellent regioselectivity was also observed in dialkoxy benzene derivatives under mild conditions.

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