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Ethanol, 2-(4-methoxy-2-nitrophenoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109364-96-7

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109364-96-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109364-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,3,6 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 109364-96:
(8*1)+(7*0)+(6*9)+(5*3)+(4*6)+(3*4)+(2*9)+(1*6)=137
137 % 10 = 7
So 109364-96-7 is a valid CAS Registry Number.

109364-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2'-(4-methoxy-2-nitrophenoxy)ethanol

1.2 Other means of identification

Product number -
Other names 2'-(4-methoxy-3-nitrophenoxy)ethanol

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:109364-96-7 SDS

109364-96-7Downstream Products

109364-96-7Relevant academic research and scientific papers

2, 4- DI (PHENYLAMINO) PYRIMIDINES USEFUL IN THE TREATMENT OF NEOPLASTIC DISEASES, INFLAMMATORY AND IMMUNE SYSTEM DISORDERS

-

Page 118; 129, (2010/02/08)

Novel pyrimidine derivatives of formula (I), to processes for their production, their use as pharmaceuticals in the treatment of neoplastic diseases, inflammatory and immune system disorders and to pharmaceutical compositions comprising them.

Selective nitration versus oxidative dealkylation of hydroquinone ethers with nitrogen dioxide

Rathore,Bosch,Kochi

, p. 6727 - 6758 (2007/10/02)

Various alkyl-substituted p-dialkoxybenzenes (ArH) react readily with nitrogen dioxide (NO2) in dichloromethane solution via either nitration (ArNO2) or oxidative dealkylation to quinones (Q). Spectral transients indicate that these coupled processes proceed from the dialkoxybenzene radical cation (ArH+) formed as the common reactive intermediate from electron-transfer in the disproportionated precursor [ArH, NO+]NO3-. In fast subsequent steps, ArH+ undergoes homolytic coupling with NO2 (which leads to aromatic nitration) and nucleophilic attack of NO3- (which results in oxidative dealkylation). As such, the competition between nitration and oxidative dealkylation is effectively modulated by solvent polarity and added nitrate.

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