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4,5-DIETHOXY-2-NITROANILINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113475-65-3

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113475-65-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113475-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,4,7 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 113475-65:
(8*1)+(7*1)+(6*3)+(5*4)+(4*7)+(3*5)+(2*6)+(1*5)=113
113 % 10 = 3
So 113475-65-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H14N2O4/c1-3-15-9-5-7(11)8(12(13)14)6-10(9)16-4-2/h5-6H,3-4,11H2,1-2H3

113475-65-3SDS

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 4,5-Diethoxy-2-nitroaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,4,5-diethoxy-2-nitro

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:113475-65-3 SDS

113475-65-3Relevant academic research and scientific papers

Benzocrown Derivatives as Ionophores for Alkali Cations, II. - Synthesis and Comparison of Urethane-, Ether-, and Ester-Linked Bis-Crown Compounds and Several "Crown-Ring Free" Analogues

Toeke, Laszlo,Bitter, Istvan,Agai, Bela,Hell, Zoltan,Lindner, Ernoe,et al.

, p. 549 - 554 (2007/10/02)

Nitro derivatives of bis-crown ethers with urethane (2), ether (10), and ester (9, 16) linkage not being able to form hydrogen bridges were synthesized, and their K(1+) selectivities were determined.A remarkable effect of the NO2 group on the selectivity was observed when a NO2***NH hydrogen bond could be formed while the others showed only slight improvement in general electroanalytical parameters.Several analogues without the crown ether ring (25, 26) were also prepared, but these compounds lost their alkaline ionophore properties.

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