922-13-4

Basic information

• Product Name: N,N-diethylpentanamide
• Synonyms: N,N-diethylpentanamide
• CAS NO: 922-13-4
• Molecular Formula: C₉H₁₉NO
• Molecular Weight: 0
• Mol File: 922-13-4.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 220.4°Cat760mmHg
• Flash Point: 83°C
• Appearance: /
• Density: 0.866g/cm³
• Vapor Pressure: 0.113mmHg at 25°C
• Refractive Index: 1.436
• CAS DataBase Reference: N,N-diethylpentanamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-diethylpentanamide(922-13-4)
• EPA Substance Registry System: N,N-diethylpentanamide(922-13-4)

Safety Data

• Hazardous Substances Data: 922-13-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C9H19NO/c1-4-7-8-9(11)10(5-2)6-3/h4-8H2,1-3H3

Upstream product

• 109-89-7 diethylamine 
• 109-52-4 valeric acid 
• 2008-34-6 2-(pentylthio)tetrahydro-2H-pyran 
• 5309-99-9 N,N-diethylthiopentanamide 
• 20605-40-7 thiobenzoylhydrazine 
• 109-72-8 n-butyllithium 
• 88-10-8 N,N-diethylcarbamyl chloride 
• 14273-07-5 1-ethoxy-pent-1-yne 
• 110-87-2 3,4-dihydro-2H-pyran 
• 693-04-9 butyl magnesium bromide 
• 638-29-9 n-valeryl chloride 
• 924-31-2 1-Diaethylamino-pent-1-in 
• 41949-84-2 2-Diethylaminotetrahydropyran 

Downstream Products

• 54007-33-9 N-ethyl-pentanamide 
• 5309-99-9 N,N-diethylthiopentanamide 
• 108-29-2 5-methyl-dihydro-furan-2-one 
• 109-52-4 valeric acid 
• 502-56-7 nonanone-5 

Relevant articles and documents

Access to Diarylmethanols by Wittig Rearrangement of ortho-, meta-, and para-Benzyloxy- N-Butylbenzamides

The N-butyl amide group, CONHBu, has been found to be an effective promoter of the [1,2]-Wittig rearrangement of aryl benzyl ethers and thus allow the two-step synthesis of isomerically pure substituted diarylmethanols starting from simple hydroxybenzoic acid derivatives. The method is compatible with a wide range of functional groups including methyl, methoxy, and fluoro, although not with nitro and, unexpectedly, is applicable to meta as well as ortho and para isomeric series.

Preparation of tertiary amides from carbamoyl chlorides and organocuprates

(Chemical Equation Presented) Reaction of carbamoyl chlorides with cyano-Gilman cuprates affords tertiary amides in good to excellent yields. The reaction is general due to the possibility of using reagents made either from organolithium or from Grignard compounds. The characterization of the main side products allowed for the suggestion of a possible mechanism.

HETEROCYCLIZATION OF DERIVATIVES OF THIONCARBOXYLIC ACIDS TO 1,3,4-THIADIAZOLES UNDER THE ACTION OF TERT-BUTYL HYPOCHLORITE

A method for synthesis of 2-alkyl-5-aryl- and 2,5-diaryl-1,3,4-thiadiazoles by successive reaction of thioamides with tert-butyl hypochlorite and benzothiohydrazides was developed.The first step in the formation of 1,3,4-thiadiazoles consists of oxidation