227180-20-3

Basic information

• Product Name: 2,2-dimethyl-N-<4-iodo-6-methoxy-3-pyridinyl>propanamide
• CAS NO: 227180-20-3
• Molecular Weight: 334.157
• Mol File: 227180-20-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2,2-dimethyl-N-<4-iodo-6-methoxy-3-pyridinyl>propanamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-dimethyl-N-<4-iodo-6-methoxy-3-pyridinyl>propanamide(227180-20-3)
• EPA Substance Registry System: 2,2-dimethyl-N-<4-iodo-6-methoxy-3-pyridinyl>propanamide(227180-20-3)

Safety Data

• Hazardous Substances Data: 227180-20-3(Hazardous Substances Data)

Upstream product

• 6628-77-9 6-methoxy-pyridin-3-ylamine 
• 3282-30-2 pivaloyl chloride 
• 227180-19-0 2,2-dimethyl-N-<5-(2-methoxypyridinyl)>propanamide 

Downstream Products

• 227180-21-4 4-iodo-6-methoxypyridin-3-ylamine 
• 227180-22-5 5-amino-2-methoxy-4-<2-(1,1,1-trimethylsilyl)-1-ethynyl>pyridine 
• 227180-23-6 3-formyl-5-methoxy-1H-pyrrolo<2,3-c>pyridine 

Relevant articles and documents

Synthesis of new melatoninergic ligands including azaindole moiety

A novel series of melatonin analogues, based on the azaindole nucleus is described. These compounds are prepared in several steps directly from the commercial available 7-azaindole or from substituted amino-, iodo- or/and nitropyridines using a catalysed palladium reaction or vicarious nucleophilic substitution of hydrogen (VNS) in order to elaborate the 6-, 5- and 4- azaindole derivatives respectively.

AZA-INDOLES AND RELATED COMPOUNDS HAVING SPHINGOSINE-1-PHOSPHATE (S1P) RECEPTOR ANTAGONIST BIOLOGICAL ACTIVITY

The present invention provides compounds are disclosed herein having the formula: Wherein n is 1 or 2; m is 0 or 1; p is 0, 1 or 2; R1 is aryl, heteroaryl or alkyl; R2 is C1-6 hydrocarbyl, alkylacyl or hydroxyalkyl; R