cas 37033-93-5|| where to buy 5-Ethyl-1H-indole-2-carboxylic acid

Product Name:5-Ethyl-1H-indole-2-carboxylic acid

IUPAC Name:5-ethyl-1H-indole-2-carboxylic acid

: CAS：37033-93-5; Molecular Formula：C11H11NO2; Purity：95%+

: Catalog Number：CM240401; Molecular Weight：189.21

Packing Unit	Available Stock	Price($)	Quantity
CM240401-5g	3-4 Weeks	ƀțŴ

Inquiry: sales@chemenu.com

For R&D use only.

Inquiry Form

Chemical Name

CAS Number

Quantity*

Required Specifications*
(Assay %, Material Grade etc.)

Contact Name*

Contact Email*

Additional Notes

Verification code*

refresh

Product Details

: CAS NO:37033-93-5; Molecular Formula:C11H11NO2; Melting Point:-; Smiles Code:O=C(C(N1)=CC2=C1C=CC(CC)=C2)O; Density:

: Catalog Number:CM240401; Molecular Weight:189.21; Boiling Point:; MDL No:MFCD00065293; Storage:

Category Infos

: Indoles; Indole is a compound of pyrrole and benzene in parallel, also known as benzopyrrole. There are two combinations of pyrrole and benzene, called indole and isoindole, respectively. Many derivatives of indole have physiological and pharmacological activities, and can synthesize vasodilators, antihistamines, antipyretic analgesics, etc. in medicine, so indole is also a very important heterocyclic compound.; indole company; As a indole company,we sincerely welcome the new and old friends from home and abroad to synergize with our company and share the benefits and opportunities.

Column Infos

: Indoles

Product Other Information

Product Overview	5-Ethyl-1H-indole-2-carboxylic acid is an important organic molecule that is used in a variety of applications. It is a heterocyclic compound that contains a nitrogen atom and is a derivative of indole.
Synthesis Method	One of the most common methods is the reaction of ethyl bromide with indole in the presence of a strong base, such as potassium hydroxide. This reaction yields 5-ethyl-1H-indole-2-carboxylic acid as the major product, along with a variety of other minor products. Another method involves the reaction of ethyl iodide with indole in the presence of a strong base. This reaction yields 5-ethyl-1H-indole-2-carboxylic acid as the major product, along with a variety of other minor products.
Chemical Properties	5-ethyl-1H-indole-2-carboxylic acid can be toxic if handled improperly. It is relatively easy to synthesize and is relatively stable.
Synthesis and Application	It has been used in the synthesis of a variety of compounds, including drugs, dyes, and fragrances. In addition, 5-ethyl-1H-indole-2-carboxylic acid has been used in the synthesis of a number of compounds that have been used in scientific research applications. For example, 5-ethyl-1H-indole-2-carboxylic acid has been used in the synthesis of indole derivatives, which have been used in the treatment of various diseases. In addition, 5-ethyl-1H-indole-2-carboxylic acid has been used in the synthesis of compounds that have been used in the study of enzyme inhibition, protein-protein interactions, and other biological processes.
Future Directions	Further research is needed to better understand its mechanism of action and the biochemical and physiological effects it has on the body. In addition, further research is needed to develop more efficient and cost-effective methods of synthesizing 5-ethyl-1H-indole-2-carboxylic acid. Finally, further research is needed to better understand the role of 5-ethyl-1H-indole-2-carboxylic acid in the treatment of various diseases.