Azelamide, N,N,N',N'-tetramethyl-

Base Information

Chemical Name:Azelamide, N,N,N',N'-tetramethyl-
CAS No.:13424-87-8
Molecular Formula:C₁₃H₂₆N₂O₂
Molecular Weight:242.362
Hs Code.:
DSSTox Substance ID:DTXSID10158607
Nikkaji Number:J54.657G
Wikidata:Q83026905
Mol file:13424-87-8.mol

Synonyms:N,N,N',N'-tetramethylnonanediamide;AZELAMIDE, N,N,N',N'-TETRAMETHYL-;13424-87-8;Tetramethylazelamide;BRN 1874596;Nonanediamide, N,N,N',N'-tetramethyl-;N,N,N',N'-tetramethyl-nonanediamide;Tetramethylazelaic diamide;DTXSID10158607;N,N,N/',N/'-Tetramethylnonanediamide;LS-22784

Suppliers and Price of Azelamide, N,N,N',N'-tetramethyl-

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

American Custom Chemicals Corporation
TETRAMETHYLAZELAMIDE 95.00%
5MG
$ 503.47

Total 4 raw suppliers

Chemical Property of Azelamide, N,N,N',N'-tetramethyl-

Chemical Property:

Vapor Pressure:8.05E-06mmHg at 25°C
Melting Point:40-41 °C
Refractive Index:1.4365 (estimate)
Boiling Point:375°Cat760mmHg
PKA:-0.13±0.70(Predicted)
Flash Point:151.1°C
PSA：40.62000
Density:0.962g/cm³
LogP:1.89350
Water Solubility.:945.20g/L(30 oC)
XLogP3:1.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:8
Exact Mass:242.199428076
Heavy Atom Count:17
Complexity:214

Purity/Quality:

97% ^*data from raw suppliers

TETRAMETHYLAZELAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C)C(=O)CCCCCCCC(=O)N(C)C

Technology Process of Azelamide, N,N,N',N'-tetramethyl-

There total 4 articles about Azelamide, N,N,N',N'-tetramethyl- 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:

: 628-77-3
1,5-diiodopentane

: 13424-87-8
Tetramethyl-azelamid

Guidance literature:: Multi-step reaction with 2 steps

1: acetonitrile

2: aq. NaOH

With sodium hydroxide; In acetonitrile;
DOI:10.1021/jo00921a013