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1-ethoxy-2,4-dimethylbenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35338-30-8

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35338-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35338-30-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,3 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 35338-30:
(7*3)+(6*5)+(5*3)+(4*3)+(3*8)+(2*3)+(1*0)=108
108 % 10 = 8
So 35338-30-8 is a valid CAS Registry Number.

35338-30-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-ethoxy-2,4-dimethylbenzene

1.2 Other means of identification

Product number -
Other names 2,4-dimethyl-phenetole

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:35338-30-8 SDS

35338-30-8Downstream Products

35338-30-8Relevant academic research and scientific papers

Transition-Metal-Free C-C, C-O, and C-N Cross-Couplings Enabled by Light

Liu, Wenbo,Li, Jianbin,Querard, Pierre,Li, Chao-Jun

, p. 6755 - 6764 (2019/05/06)

Transition-metal-catalyzed cross-couplings to construct C-C, C-O, and C-N bonds have revolutionized chemical science. Despite great achievements, these metal catalysts also raise certain issues including their high cost, requirement of specialized ligands, sensitivity to air and moisture, and so-called "transition-metal-residue issue". Complementary strategy, which does not rely on the well-established oxidative addition, transmetalation, and reductive elimination mechanistic paradigm, would potentially eliminate all of these metal-related issues. Herein, we show that aryl triflates can be coupled with potassium aryl trifluoroborates, aliphatic alcohols, and nitriles without the assistance of metal catalysts empowered by photoenergy. Control experiments reveal that among all common aryl electrophiles only aryl triflates are competent in these couplings whereas aryl iodides and bromides cannot serve as the coupling partners. DFT calculation reveals that once converted to the aryl radical cation, aryl triflate would be more favorable to ipso substitution. Fluorescence spectroscopy and cyclic voltammetry investigations suggest that the interaction between excited acetone and aryl triflate is essential to these couplings. The results in this report are anticipated to provide new opportunities to perform cross-couplings.

Streamlined synthesis of the bippyphos family of ligands and cross-coupling applications

Withbroe, Gregory J.,Singer, Robert A.,Sieser, Janice E.

, p. 480 - 489 (2013/01/03)

We describe the efficient preparation of Bippyphos, 1. The key precursor to Bippyphos, 5, was prepared via a one-pot bromination of diketone 2 followed by alkylation with pyrazole and condensation with phenylhydrazine. Lithiation of 5 and trapping with ditert-butylchlorophosphine afforded Bippyphos, 1. Using this approach we have prepared several derivatives of Bippyphos to probe the structure and activity relationships of this family of phosphine ligands. We also demonstrate the utility of these ligands in Pdcatalyzed amination reactions and other cross-coupling reactions.

A New Rearrangement of Alkoxybenzyl Anions

Bates, Robert B.,Siahaan, Teruna J.,Suvannachut, Kessara

, p. 1328 - 1334 (2007/10/02)

Alkyl groups migrate from oxygen to carbon in alkyl aryl ethers which have been metalated in benzylic positions. 2,6-Dimethylanisole provides a variety of 2,6-dialkylphenols and their ethers in 45-80percent yields.Rearrangement products are obtained in 10-30percent yields from other dimethylanisoles and from methylanisoles.The reactions appear to proceed, like Wittig rearrangements, by homolytic cleavage of the alkyl-oxygen bond followed by recombination of the resulting radical pair in a different way.The rearrangements can be avoided by using methyl ethers and working at or below room temperature.

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