N,N'-bis(6-aminohexyl)hexanediamide

Base Information

Chemical Name:N,N'-bis(6-aminohexyl)hexanediamide
CAS No.:65170-34-5
Molecular Formula:C18H38N4O2
Molecular Weight:342.525
Hs Code.:
DSSTox Substance ID:DTXSID00398439
Wikidata:Q82200392

Synonyms:N,N'-bis(6-aminohexyl)hexanediamide;65170-34-5;SCHEMBL8995394;DTXSID00398439

Suppliers and Price of N,N'-bis(6-aminohexyl)hexanediamide

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 9 raw suppliers

Chemical Property of N,N'-bis(6-aminohexyl)hexanediamide

Chemical Property:

XLogP3:0.4
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:17
Exact Mass:342.29947647
Heavy Atom Count:24
Complexity:281

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C(CCCNC(=O)CCCCC(=O)NCCCCCCN)CCN

Technology Process of N,N'-bis(6-aminohexyl)hexanediamide

There total 8 articles about N,N'-bis(6-aminohexyl)hexanediamide 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: 72.0%

: 65170-34-5
BAHA

Guidance literature:: at 65 ℃; for 6h; Inert atmosphere;

Reference yield:

: 543740-23-4
{6-[5-(6-tert-butoxycarbonylamino-hexylcarbamoyl)-pentanoylamino]-hexyl}-carbamic acid tert-butyl ester

: 65170-34-5
BAHA

Guidance literature:: With trifluoroacetic acid; at 20 ℃;
DOI:10.1039/b207872d

Reference yield:

: 51857-17-1
tert-butyl N-(6-aminohexyl)carbamate

: 65170-34-5
BAHA

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / CHCl₃ / 20 °C

2: trifluoroacetic acid / 20 °C

With trifluoroacetic acid; In chloroform;
DOI:10.1039/b207872d