41116-48-7

Basic information

• Product Name: 4-Pyridinecarboxamide,N-ethyl-(9CI)
• Synonyms: 4-Pyridinecarboxamide,N-ethyl-(9CI);N-Ethyl-4-pyridinecarboxaMide;4-PyridinecarboxaMide, N-ethyl-;N-Ethylisonicotinamide
• CAS NO: 41116-48-7
• Molecular Formula: C8H10N2O
• Molecular Weight: 150.1778
• Product Categories: AMIDE
• Mol File: 41116-48-7.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Pyridinecarboxamide,N-ethyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Pyridinecarboxamide,N-ethyl-(9CI)(41116-48-7)
• EPA Substance Registry System: 4-Pyridinecarboxamide,N-ethyl-(9CI)(41116-48-7)

Safety Data

• Hazardous Substances Data: 41116-48-7(Hazardous Substances Data)

Upstream product

• 55-22-1 pyridine-4-carboxylic acid 
• 75-09-2 dichloromethane 
• 75-04-7 ethylamine 
• 2459-09-8 4-pyridinecarboxylic acid, methyl ester 
• 1453-82-3 isonicotinamide 
• 557-66-4 ethanamine hydrochloride 
• 39178-35-3 isonicotinoyl chloride hydrochloride 
• 1570-45-2 isonicotinic acid ethylester 

Downstream Products

• 1903-65-7 piperidine-4-carboxylic acid ethylamide 

Relevant articles and documents

Generation of alkyl radicals from alkylsilyl peroxides and their applications to C-N or C-O bond formations

This article describes a novel method for the generation of alkyl radicals from alkylsilyl peroxides and their applications to the Cu-catalyzed mono-N-alkylation of amides or arylamines, and to the O-alkylation of carboxylic acids. The use of alkylsilyl peroxides as alkyl radical sources includes the following synthetic advantages: i) various alkylsilyl peroxides can be readily synthesized from the corresponding alcohols and be stored at bench, and ii) a variety of alkyl radicals can be generated efficiently under mild conditions.

Fungicides for the control of take-all disease of plants

A method of controlling Take-All disease of plants by applying a fungicide of the formula STR1 wherein Z1 and Z2 are C and are part of an aromatic ring which is benzothiophene; and A is selected from --C(X)-amine wherein the amine is an unsubstituted, monosubstituted or disubstituted amino radical, --C(O)--SR3, --NH--C(X)R4, and --C(=NR3)--XR7 ; B is --Wm --Q(R2)3 or selected from O-tolyl, 1-naphthyl, 2-naphthyl, and 9-phenanthryl, each optionally substituted with halogen or R4 ; Q is C, Si, Ge, or Sn; W is --C(R3)p H(2-p) --; or when Q is C, W is selected from --C(R3)p H(2-p), --N(R3)m H(1-m)--, --S(O)p--, and --O--; X is 0 or S; n is 0, 1, 2, or 3; m is 0 or 1; p is 0, 1, or 2; each R and R2 is independently defined herein; R3 is C1 -C4 alkyl; R4 is C1 -C4 alkyl, haloalkyl, alkoxy, alkylthio, alkylamino, or dialkylamino; and R7 is C1 -C4 alkyl, haloalkyl, or phenyl, optionally substituted with halo, nitro, or R4 ; or an agronomic salt thereof.

4-Piperidino-2-phenylquinolines

Disclosed are compounds of the formula STR1 wherein: R1 and R2 may be either the same or different and each is hydrogen or lower alkyl; and wherein R3 and R4 may be either the same or different and each is hydrogen, halogen, or lower alkyl, with the proviso that R3 and R4 cannot both be hydrogen. These compounds are useful as anticonvulsant or anxiolytic agents.