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2,3-Dimethyl-5-methoxyphenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34883-01-7

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34883-01-7 Usage

Uses

5-Methoxy-2,3-dimethylphenol can be as potential coffee beans’ markers.

Check Digit Verification of cas no

The CAS Registry Mumber 34883-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,8,8 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34883-01:
(7*3)+(6*4)+(5*8)+(4*8)+(3*3)+(2*0)+(1*1)=127
127 % 10 = 7
So 34883-01-7 is a valid CAS Registry Number.

34883-01-7SDS

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 5-Methoxy-2,3-dimethylphenol

1.2 Other means of identification

Product number -
Other names 2,3-Dimethyl-5-methoxyphenol

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:34883-01-7 SDS

34883-01-7Relevant academic research and scientific papers

Synthesis of substituted resorcinol monomethyl ethers from 2-bromo-3-methoxycyclohex-2-en-1-ones

Shao, Wenjie,Clive, Derrick L. J.

, p. 3211 - 3216 (2015/03/30)

2-Bromo-3-methoxycyclohex-2-en-1-ones are readily alkylated at C-6 with reactive halides, and then treatment with DBU (2 equiv) in PhMe at room temperature results in smooth loss of bromide and aromatization to resorcinol monomethyl ethers of defined substitution pattern.

Synthesis of tetra- and pentasubstituted benzenes from dimedone and derivatives

Nelson,Nelson

, p. 1287 - 1290 (2007/10/02)

Treatment of dimedone (5,5-dimethylcyclohexane-1,3-dione) and derivatives with one molar equivalent of sulfuric acid in trifluoroacetic anhydride leads, via sulfonation and a 1,2-methyl group migration, to a variety of dimethylresorcinol derivatives. The

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