5585-96-6 | 4-Acetoxyindole

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$12.00	$8.00
1g	98%	in stock	$13.00	$9.00
5g	98%	in stock	$29.00	$20.00
10g	98%	in stock	$56.00	$39.00
25g	98%	in stock	$108.00	$75.00

Description

• Catalog Number: AB67706
• Chemical Name: 4-Acetoxyindole
• CAS Number: 5585-96-6
• Molecular Formula: C10H9NO2
• Molecular Weight: 175.1840
• MDL Number: MFCD00010678
• SMILES: CC(=O)Oc1cccc2c1cc[nH]2

Computed Properties

• Complexity: 205
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 2
• XLogP3: 1.8

Upstream Synthesis Route

1H-Indol-4-yl acetate, also known as indole-4-acetic acid, is a versatile compound widely used in chemical synthesis. In organic chemistry, it serves as a key intermediate in the production of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure containing an indole ring and an acetate group imparts valuable properties that make it a valuable building block in the synthesis of biologically active molecules. 1H-Indol-4-yl acetate is particularly crucial in the development of new drugs due to its ability to modulate biological pathways and exhibit potent pharmacological activities. Furthermore, in the field of agrochemicals, this compound plays a significant role in the formulation of plant growth regulators and herbicides. Its influence on plant growth and development makes it an essential component in enhancing crop yield and quality. In summary, 1H-Indol-4-yl acetate is a key player in chemical synthesis, enabling the creation of diverse compounds with significant applications in the pharmaceutical, agricultural, and materials industries. Its versatility and reactivity make it an indispensable tool for researchers and chemists striving to innovate and advance their respective fields.

Literature

• Indolealkylamines: biotransformations and potential drug-drug interactions.

  The AAPS journal 20080601