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(5-amino-2-methoxyphenoxy)acetic acid ethyl ester is an organic compound derived from the amino acid glycine, featuring a phenyl ring with a methoxy group and an amino group attached to the carbon atom, along with a carboxylic acid group and an ethyl ester functional group. Its unique structure and properties may offer potential applications in various fields.

41428-22-2

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41428-22-2 Usage

Uses

Used in Pharmaceutical Industry:
(5-amino-2-methoxyphenoxy)acetic acid ethyl ester is used as a potential candidate in drug development for its unique molecular structure that may interact with biopolymers and macromolecules, offering new avenues for therapeutic applications.
Used in Agrochemical Industry:
(5-amino-2-methoxyphenoxy)acetic acid ethyl ester is used as a potential ingredient in the development of herbicides, leveraging its specific interactions with biological targets to control weed growth effectively.
Used in Material Sciences:
(5-amino-2-methoxyphenoxy)acetic acid ethyl ester is used as a building block in material synthesis, where its unique properties can be harnessed to create novel materials with specific characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 41428-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,2 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41428-22:
(7*4)+(6*1)+(5*4)+(4*2)+(3*8)+(2*2)+(1*2)=92
92 % 10 = 2
So 41428-22-2 is a valid CAS Registry Number.

41428-22-2Relevant academic research and scientific papers

Quinazolines: Combined type 3 and 4 phosphodiesterase inhibitors

Charpiot, Brigitte,Brun, Jvan,Donze, Irene,Naef, Reto,Stefani, Monique,Mueller, Thomas

, p. 2891 - 2896 (2007/10/03)

A series of quinazolines has been prepared and evaluated for its ability to inhibit cyclic AMP phosphodiesterase type 3, type 4A, 4B and 4D. The most potent inhibitors showed IC50 values in the nanomolar range for type 3 and type 4 isoforms and bind with high affinity to the [3H]rolipram binding site. These quinazolines represent a new family of potent mixed PDE 3 / 4 inhibitors and are expected to have a therapeutic potential.

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