2,6-Diamino-N-hydroxyhexanamide

Base Information

Chemical Name:2,6-Diamino-N-hydroxyhexanamide
CAS No.:4383-81-7
Molecular Formula:C₆H₁₅N₃O₂
Molecular Weight:161.204
Hs Code.:
Nikkaji Number:J1.781.830I

Synonyms:2,6-Diamino-N-hydroxyhexanamide;Hexanamide, 2,6-diamino-N-hydroxy-;4383-81-7;C6-H15-N3-O2;SCHEMBL11771047;2,6-Diaminohexanehydroxamic acid

Suppliers and Price of 2,6-Diamino-N-hydroxyhexanamide

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 1 raw suppliers

Chemical Property of 2,6-Diamino-N-hydroxyhexanamide

Chemical Property:

Density:1.161g/cm³
XLogP3:-1.7
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:161.116426730
Heavy Atom Count:11
Complexity:118

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C(CCN)CC(C(=O)NO)N

Technology Process of 2,6-Diamino-N-hydroxyhexanamide

There total 3 articles about 2,6-Diamino-N-hydroxyhexanamide 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:

: 687-64-9
L-lysine methyl ester

: 25125-92-2,4383-81-7
L-Lysin-hydroxamsaeure

Guidance literature:: With potassium hydroxide; hydroxylamine hydrochloride; In methanol;
DOI:10.1021/ja01500a035

Reference yield:

: 56-87-1,3506-25-0
L-lysine

: 25125-92-2,4383-81-7
L-Lysin-hydroxamsaeure

Guidance literature:: With hydroxylamine; In water; at 37 ℃; for 16h; Product distribution; pH = 5.2; effect of metal ions and organic phosphates on hydroxamate formation;