Ethyl (3-formyl-2-methyl-1H-indol-1-yl)acetate is a chemical compound with the molecular formula C13H15NO3. It is an ester derivative of indole, a heterocyclic aromatic organic compound. ethyl (3-formyl-2-methyl-1H-indol-1-yl)acetate features an indole ring, a formyl group, and an acetate group, which together confer a unique and potentially useful chemical profile. It possesses potential biological activities and is utilized in the synthesis of various pharmaceuticals and natural products, making it a versatile component in the field of organic chemistry and drug development.
433307-59-6
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Basic information
- Product Name: ethyl (3-formyl-2-methyl-1H-indol-1-yl)acetate
- Synonyms: ethyl (3-formyl-2-methyl-1H-indol-1-yl)acetate;Albb-006899;ethyl (3-formyl-2-methyl-1H-indol-1-yl)acetate(SALTDATA: FREE);2-(3-formyl-2-methyl-1-indolyl)acetic acid ethyl ester;2-(3-formyl-2-methyl-indol-1-yl)acetic acid ethyl ester;ethyl 2-(3-formyl-2-methyl-indol-1-yl)acetate;ethyl 2-(3-formyl-2-methylindol-1-yl)acetate;ethyl 2-(3-methanoyl-2-methyl-indol-1-yl)ethanoate
- CAS NO:433307-59-6
- Molecular Formula: C14H15NO3
- Molecular Weight: 245.28
- EINECS: N/A
- Product Categories: N/A
- Mol File: 433307-59-6.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 411.9°C at 760 mmHg
- Flash Point: 202.9°C
- Appearance: /
- Density: 1.16g/cm3
- Vapor Pressure: 5.38E-07mmHg at 25°C
- Refractive Index: 1.563
- Storage Temp.: 2-8°C
- Solubility: N/A
- CAS DataBase Reference: ethyl (3-formyl-2-methyl-1H-indol-1-yl)acetate(CAS DataBase Reference)
- NIST Chemistry Reference: ethyl (3-formyl-2-methyl-1H-indol-1-yl)acetate(433307-59-6)
- EPA Substance Registry System: ethyl (3-formyl-2-methyl-1H-indol-1-yl)acetate(433307-59-6)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: IRRITANT
- PackingGroup: N/A
- Hazardous Substances Data: 433307-59-6(Hazardous Substances Data)
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433307-59-6 Usage
Uses
Used in Pharmaceutical Synthesis:Ethyl (3-formyl-2-methyl-1H-indol-1-yl)acetate is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the formation of complex molecular structures that can exhibit therapeutic effects.
Used in Natural Product Synthesis:
In the realm of natural product chemistry, ethyl (3-formyl-2-methyl-1H-indol-1-yl)acetate serves as a building block for the creation of bioactive compounds that can mimic or interact with natural substances found in plants, fungi, or other organisms.
Used in Chemical Research:
Ethyl (3-formyl-2-methyl-1H-indol-1-yl)acetate is utilized as a research compound in academic and industrial laboratories to explore its reactivity, potential applications, and to understand its role in various chemical reactions and processes.
Used in Drug Development:
As a compound with potential biological activities, ethyl (3-formyl-2-methyl-1H-indol-1-yl)acetate is used in drug development for its possible contribution to the discovery of new therapeutic agents, particularly those targeting specific biological pathways or receptors.
Check Digit Verification of cas no
The CAS Registry Mumber 433307-59-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,3,3,0 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.Calculate Digit Verification of CAS Registry Number 433307-59:
(8*4)+(7*3)+(6*3)+(5*3)+(4*0)+(3*7)+(2*5)+(1*9)=126
126 % 10 = 6
So 433307-59-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H15NO3/c1-3-18-14(17)8-15-10(2)12(9-16)11-6-4-5-7-13(11)15/h4-7,9H,3,8H2,1-2H3
433307-59-6Upstream product
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ethyl (3-formyl-2-methyl-1H-indol-1-yl)acetate
