(5-Chloro-1H-indol-2-yl)methanol

≥98%

  • Product Code: 57368
  CAS:    53590-47-9
Molecular Weight: 181.62 g./mol Molecular Formula: C₉H₈ClNO
EC Number: MDL Number: MFCD19301593
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, away from light, dry, sealed
Product Description: (5-Chloro-1H-indol-2-yl)methanol is primarily utilized in organic synthesis as a key intermediate for the development of various pharmaceutical compounds. Its structure, featuring both an indole ring and a hydroxymethyl group, makes it a versatile building block in the synthesis of bioactive molecules. It is often employed in the preparation of potential drug candidates targeting neurological disorders, including serotonin receptor modulators, due to the indole moiety's resemblance to serotonin. Additionally, it serves as a precursor in the synthesis of complex heterocyclic compounds used in medicinal chemistry research. Its applications extend to the development of agrochemicals, where it contributes to the creation of novel pesticides and herbicides. The compound’s reactivity also allows for further functionalization, enabling its use in the design of specialized organic materials.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿1,116.00
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0.250 10-20 days ฿2,088.00
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1.000 10-20 days ฿5,751.00
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(5-Chloro-1H-indol-2-yl)methanol
(5-Chloro-1H-indol-2-yl)methanol is primarily utilized in organic synthesis as a key intermediate for the development of various pharmaceutical compounds. Its structure, featuring both an indole ring and a hydroxymethyl group, makes it a versatile building block in the synthesis of bioactive molecules. It is often employed in the preparation of potential drug candidates targeting neurological disorders, including serotonin receptor modulators, due to the indole moiety's resemblance to serotonin. Additionally, it serves as a precursor in the synthesis of complex heterocyclic compounds used in medicinal chemistry research. Its applications extend to the development of agrochemicals, where it contributes to the creation of novel pesticides and herbicides. The compound’s reactivity also allows for further functionalization, enabling its use in the design of specialized organic materials.
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