N,N-diethylheptanamide

Base Information

Chemical Name:N,N-diethylheptanamide
CAS No.:10385-08-7
Molecular Formula:C11H23 N O
Molecular Weight:185.31
Hs Code.:
NSC Number:195011
DSSTox Substance ID:DTXSID80307766
Nikkaji Number:J3.009.749A
Wikidata:Q82055309
Mol file:10385-08-7.mol

Synonyms:NSC195011;10385-08-7;N,N-diethylheptanamide;SCHEMBL6117074;DTXSID80307766;AKOS003854141;NSC-195011

Suppliers and Price of N,N-diethylheptanamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 6 raw suppliers

Chemical Property of N,N-diethylheptanamide

Chemical Property:

Vapor Pressure:0.0268mmHg at 25°C
Boiling Point:246.6°Cat760mmHg
Flash Point:92.5°C
Density:0.863g/cm³
XLogP3:2.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:7
Exact Mass:185.177964357
Heavy Atom Count:13
Complexity:130

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCC(=O)N(CC)CC

Technology Process of N,N-diethylheptanamide

There total 10 articles about N,N-diethylheptanamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 91.0%

: 111-71-7
heptanal

: 109-89-7
diethylamine

: 10385-08-7
heptanoic acid diethylamide

Guidance literature:: heptanal; diethylamine; With N-chloro-succinimide; In dichloromethane; Inert atmosphere; Cooling with ice;

With 5a(S),10b(R)-5a,10b-dihydro-2-(pentafluorophenyl)-4H,6H-indeno[2,1-b][1,2,4]triazolo[4,3-d][1,4]oxazinium tetrafluoroborate; benzotriazol-1-ol; triethylamine; In dichloromethane; at 20 ℃; chemoselective reaction; Inert atmosphere;
DOI:10.1039/c1cc15539c