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

97%

  • Product Code: 37308
  CAS:    1131737-05-7
Molecular Weight: 190.07 g./mol Molecular Formula: C₈H₉Cl₂N
EC Number: MDL Number: MFCD06762211
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
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.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days $1,110.65
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(R)-1-(2,6-Dichlorophenyl)ethanamine
(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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