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6-Amino-3,4-diethoxybenzoic Acid, with the molecular formula C11H15NO4, is a specialized chemical compound that features a benzene ring as the base for the benzoic acid component. The 6-amino and 3,4-diethoxy parts indicate the substitution of hydrogen atoms in the benzene ring. It is used in the synthesis of various chemical products and as a research compound.

20197-72-2

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20197-72-2 Usage

Uses

Used in Chemical Synthesis:
6-Amino-3,4-diethoxybenzoic Acid is used as a key intermediate in the synthesis of a wide range of chemical products. Its unique structure allows for the creation of various derivatives, making it a valuable component in the development of new compounds.
Used in Research Applications:
6-Amino-3,4-diethoxybenzoic Acid is employed as a research compound, facilitating the study of its properties and potential applications. This can include investigations into its chemical reactivity, stability, and interactions with other molecules, as well as its potential uses in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 20197-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,9 and 7 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20197-72:
(7*2)+(6*0)+(5*1)+(4*9)+(3*7)+(2*7)+(1*2)=92
92 % 10 = 2
So 20197-72-2 is a valid CAS Registry Number.

20197-72-2SDS

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 2-amino-4,5-diethoxybenzoic acid

1.2 Other means of identification

Product number -
Other names Anthranilic acid,4,5-diethoxy

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:20197-72-2 SDS

20197-72-2Relevant academic research and scientific papers

Quinazoline derivatives and therapeutic use thereof

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Page/Page column 18-19, (2008/06/13)

Quinazoline derivatives represented by the general formula pharmacologically acceptable salts thereof, and compositions containing such compounds are described. Methods for using the compounds for treatment of hyperproliferative disorders are also described.

Anilinodialkoxyquinazolines: Screening epidermal growth factor receptor tyrosine kinase inhibitors for potential tumor imaging probes

VanBrocklin, Henry F.,Lim, John K.,Coffing, Stephanie L.,Hom, Darren L.,Negash, Kitaw,Ono, Michele Y.,Gilmore, Jennifer L.,Bryant, Ianthe,Riese II, David J.

, p. 7445 - 7456 (2007/10/03)

The epidermal growth factor receptor (EGFR), a long-standing drug development target, is also a desirable target for imaging. Sixteen dialkoxyquinazoline analogues, suitable for labeling with positron-emitting isotopes, have been synthesized and evaluated in a battery of in vitro assays to ascertain their chemical and biological properties. These characteristics provided the basis for the adoption of a selection schema to identify lead molecules for labeling and in vivo evaluation. A new EGFR tyrosine kinase radiometric binding assay revealed that all of the compounds possessed suitable affinity (IC50 = 0.4-51 nM) for the EGFR tyrosine kinase. All of the analogues inhibited ligand-induced EGFR tyrosine phosphorylation (IC 50 = 0.8-20 nM). The HPLC-estimated octanol/water partition coefficients ranged from 2 to 5.5. Four compounds, 4-(2′-fluoroanilino)- and 4-(3′-fluoroanilino)-6,7-diethoxyquinazoline as well as 4-(3′-chloroanilino)- and 4-(3′-bromoanilino)-6,7- dimethoxyquinazoline, possess the best combination of characteristics that warrant radioisotope labeling and further evaluation in tumor-bearing mice.

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