Home > Products > 1000414-37-8

1000414-37-8
3-Benzofuranacetic acid, 2,3-dihydro-6-hydroxy-

Catalog#:1P000140

CAS:1000414-37-8

MDL:MFCD13184245

Molecular Formula:C10H10O4

Molecular Weight:194.1840

UN Number:

Haz Class:

Packing Group:

Synonyms: 1000414-37-8; 2-(6-Hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid; AKOS016002408; SB17659; KS-0000065Z; AS-53452; SC-88691; TC-164035; CS-0013206; FT-0766427; ST24021818; 2-(6-Hydroxy-2,3-dihydrobenzofuran-3-yl)acetic aci; 2-(6-hydroxy-2,3-dihydro-1-benzofuran-3-yl)acetic acid; Z2736474651; 2-(6-Hydroxy-2,3-dihydrobenzo[b]furan-3-yl)acetic acid; C10H10O4; 2,3-dihydro-6-hydroxy-3-Benzofuranacetic acid; (S)-2-(6-hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid; 1380792-92-6; 52057-89-3; (6-hydroxy-2,3-dihydro-1-benzofuran-3-yl)acetic acid; SCHEMBL204645; DTXSID50630654; XGXRWHAYNFAHBM-UHFFFAOYSA-N; 0055AA; ANW-75290; MFCD13184245;

Keywords: 1000414-37-8,MFCD13184245,1P000140,3-Benzofuranacetic acid, 2,3-dihydro-6-hydroxy-,C10H10O4

Inquire
Catalog# Purity Size Price Dis. Price Availability Quantity
1P000140 95% 250mg $80.00 $60.00 In Stock USA ADD TO CART BUY NOW
1P000140 95% 500mg $134.00 $100.00 In Stock USA ADD TO CART BUY NOW
1P000140 95% 1g $200.00 $150.00 In Stock USA ADD TO CART BUY NOW
1P000140 95% 5g $620.00 $465.00 In Stock USA ADD TO CART BUY NOW
1P000140 95% 10g $1,033.00 $775.00 In Stock USA ADD TO CART BUY NOW

  •                                        2-(6-Hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid, also known as $name$, is a versatile compound that finds wide application in chemical synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure containing a benzofuran ring coupled with an acetic acid moiety imparts distinct properties that make it valuable in various synthetic processes.In chemical synthesis, $name$ serves as a key building block for creating biologically active molecules due to its ability to participate in diverse reactions. Its hydroxy and carboxylic acid functional groups enable facile derivatization, allowing for the introduction of different substituents to modulate the compound's physicochemical and biological properties. Additionally, the presence of the benzofuran ring provides aromaticity and structural rigidity, contributing to the stability and reactivity of the molecule in reactions.Moreover, the hydroxyl group in $name$ offers potential for hydrogen bonding interactions, which can be crucial in the design of bioactive compounds that target specific biological receptors or enzymes. By utilizing the versatility of this compound in chemical synthesis, researchers can access a variety of derivatives with tailored properties for various applications in medicinal chemistry, agricultural chemistry, and materials science.In summary, the application of 2-(6-Hydroxy-2,3-dihydrobenzofuran-3-yl)acetic acid in chemical synthesis lies in its role as a versatile intermediate for constructing complex molecules with potential pharmaceutical and agrochemical significance. By harnessing its unique structural features and functional groups, chemists can exploit the compound's reactivity to access a diverse array of derivatives for innovative drug discovery and other chemical research endeavors.
                                        

Copyright C 2019 1PlusChem LLC. All Right Reserved