701260-75-5

Basic information

• Product Name: N-benzo[1,3]dioxol-5-yl-2-(4-nitrophenoxy)acetamide
• Synonyms: N-benzo[1,3]dioxol-5-yl-2-(4-nitrophenoxy)acetamide
• CAS NO: 701260-75-5
• Molecular Weight: 316.27
• Mol File: 701260-75-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-benzo[1,3]dioxol-5-yl-2-(4-nitrophenoxy)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzo[1,3]dioxol-5-yl-2-(4-nitrophenoxy)acetamide(701260-75-5)
• EPA Substance Registry System: N-benzo[1,3]dioxol-5-yl-2-(4-nitrophenoxy)acetamide(701260-75-5)

Safety Data

• Hazardous Substances Data: 701260-75-5(Hazardous Substances Data)

Upstream product

• 100-02-7 4-nitro-phenol 
• 227199-07-7 α-chloro-N-(3,4-methylenedioxyphenyl)acetamide 
• 14268-66-7 benzo[1,3]dioxolo-5-ylamine 

Downstream Products

• 936633-12-4 2-(4-aminophenoxy)-N-benzo[1,3]dioxol-5-ylacetamide 

Relevant articles and documents

N6-[(Hetero)aryl/(cyclo)alkyl-carbamoyl-methoxy-phenyl]-(2-chloro)-5′-N-ethylcarboxamido-adenosines: The first example of adenosine-related structures with potent agonist activity at the human A2B adenosine receptor

A new series of N6-[(hetero)aryl/(cyclo)alkyl-carbamoyl-methoxy-phenyl]-(2-chloro)-5′-N-ethylcarboxamido-adenosines (24-43) has been synthesised and tested in binding assays at hA1, hA2A and hA3 adenosine receptors, and in a functional assay at the hA2B subtype. The examined compounds displayed high potency in activating A2B receptors with good selectivity versus A2A subtypes. The introduction of an unsubstituted 4-[(phenylcarbamoyl)-methoxy]-phenyl chain at the N6 position of 5′-N-ethylcarboxamido-adenosine led us to the recognition of compound 24 as a full agonist displaying the highest efficacy of the series (EC50 hA2B = 7.3 nM). These compounds represent the first report about adenosine-related structures capable of activating hA2B subtype in the low nanomolar range.