1-Acetyl-5-iodo-1H-indol-3-yl acetate is a synthetic chemical compound that belongs to the class of indole derivatives. It features an indole ring with an acetyl group and an iodo substituent, which endows it with unique structural and reactivity properties. 1-Acetyl-5-iodo-1H-indol-3-yl acetate is of interest in the realms of organic synthesis and medicinal chemistry due to its potential to serve as a building block for more complex organic molecules and as a starting material for the development of new pharmaceuticals.
26490-98-2
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Basic information
- Product Name: 1-Acetyl-5-iodo-1H-indol-3-yl acetate
- Synonyms: 1-Acetyl-5-iodo-1H-indol-3-yl acetate
- CAS NO:26490-98-2
- Molecular Formula: C12H10INO3
- Molecular Weight: 343.11717
- EINECS: N/A
- Product Categories: N/A
- Mol File: 26490-98-2.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 416.4±25.0 °C(Predicted)
- Flash Point: N/A
- Appearance: /
- Density: 1.74±0.1 g/cm3(Predicted)
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 1-Acetyl-5-iodo-1H-indol-3-yl acetate(CAS DataBase Reference)
- NIST Chemistry Reference: 1-Acetyl-5-iodo-1H-indol-3-yl acetate(26490-98-2)
- EPA Substance Registry System: 1-Acetyl-5-iodo-1H-indol-3-yl acetate(26490-98-2)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 26490-98-2(Hazardous Substances Data)
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26490-98-2 Usage
Uses
Used in Organic Synthesis:1-Acetyl-5-iodo-1H-indol-3-yl acetate is used as a building block for the synthesis of complex organic molecules, leveraging its unique structure to create a variety of chemical entities.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-Acetyl-5-iodo-1H-indol-3-yl acetate is used as a starting material for the development of novel pharmaceuticals, taking advantage of its reactivity to form new compounds with potential therapeutic applications.
Used in Cross-Coupling Reactions:
The presence of the iodo substituent in 1-Acetyl-5-iodo-1H-indol-3-yl acetate makes it suitable for use in various cross-coupling reactions, which are essential for the creation of carbon-carbon and carbon-heteroatom bonds, further expanding its utility in chemical synthesis and drug discovery.
Overall, 1-Acetyl-5-iodo-1H-indol-3-yl acetate holds promise as a versatile compound in the synthesis of diverse organic compounds and contributes to drug discovery efforts through its application in multiple chemical and pharmaceutical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 26490-98-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,4,9 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.Calculate Digit Verification of CAS Registry Number 26490-98:
(7*2)+(6*6)+(5*4)+(4*9)+(3*0)+(2*9)+(1*8)=132
132 % 10 = 2
So 26490-98-2 is a valid CAS Registry Number.
26490-98-2Upstream product
26490-98-2Downstream Products
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1-Acetyl-5-iodo-1H-indol-3-yl acetate
