(3,4-Dichloro-benzylamino)-acetic acid

≥95%

Reagent Code: #36604
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CAS Number 261959-65-3

science Other reagents with same CAS 261959-65-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.08 g/mol
Formula C₉H₉Cl₂NO₂
badge Registry Numbers
MDL Number MFCD11139130
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in an inert gas

description Product Description

(3,4-Dichloro-benzylamino)-acetic acid is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active compounds. Its structure, featuring both a benzylamine and acetic acid moiety, makes it a versatile building block for the development of herbicides and fungicides, particularly in agricultural chemistry. Additionally, it is explored in medicinal chemistry for the design of potential drug candidates, especially in the synthesis of molecules targeting specific enzymes or receptors. Its dichloro-substituted aromatic ring enhances its binding affinity in certain biological systems, making it valuable in research and development of new therapeutic agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,475.00
inventory 1g
10-20 days ฿6,660.00

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(3,4-Dichloro-benzylamino)-acetic acid
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(3,4-Dichloro-benzylamino)-acetic acid is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active compounds. Its structure, featuring both a benzylamine and acetic acid moiety, makes it a versatile building block for the development of herbicides and fungicides, particularly in agricultural chemistry. Additionally, it is explored in medicinal chemistry for the design of potential drug candidates, especially in the s

(3,4-Dichloro-benzylamino)-acetic acid is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active compounds. Its structure, featuring both a benzylamine and acetic acid moiety, makes it a versatile building block for the development of herbicides and fungicides, particularly in agricultural chemistry. Additionally, it is explored in medicinal chemistry for the design of potential drug candidates, especially in the synthesis of molecules targeting specific enzymes or receptors. Its dichloro-substituted aromatic ring enhances its binding affinity in certain biological systems, making it valuable in research and development of new therapeutic agents.

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