(R)-1-(2,6-Dichlorophenyl)ethanamine

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Reagent Code: #37308
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CAS Number 1131737-05-7

science Other reagents with same CAS 1131737-05-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.07 g/mol
Formula C₈H₉Cl₂N
badge Registry Numbers
MDL Number MFCD06762211
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(R)-1-(2,6-Dichlorophenyl)ethanamine is primarily utilized in the pharmaceutical industry as a chiral intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its enantiomeric purity is particularly valuable in the development of drugs that require specific stereochemistry for optimal therapeutic efficacy. This compound is often employed in the production of analgesics and anti-inflammatory agents, where its structure contributes to the binding affinity and selectivity of the final drug molecule. Additionally, it serves as a key building block in the synthesis of compounds targeting neurological disorders, leveraging its ability to interact with specific receptors in the central nervous system. Its applications are also explored in agrochemical research for the development of chiral pesticides and herbicides.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿22,113.00

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(R)-1-(2,6-Dichlorophenyl)ethanamine
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(R)-1-(2,6-Dichlorophenyl)ethanamine is primarily utilized in the pharmaceutical industry as a chiral intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its enantiomeric purity is particularly valuable in the development of drugs that require specific stereochemistry for optimal therapeutic efficacy. This compound is often employed in the production of analgesics and anti-inflammatory agents, where its structure contributes to the binding affinity and selectivity of the fi

(R)-1-(2,6-Dichlorophenyl)ethanamine is primarily utilized in the pharmaceutical industry as a chiral intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its enantiomeric purity is particularly valuable in the development of drugs that require specific stereochemistry for optimal therapeutic efficacy. This compound is often employed in the production of analgesics and anti-inflammatory agents, where its structure contributes to the binding affinity and selectivity of the final drug molecule. Additionally, it serves as a key building block in the synthesis of compounds targeting neurological disorders, leveraging its ability to interact with specific receptors in the central nervous system. Its applications are also explored in agrochemical research for the development of chiral pesticides and herbicides.

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