6-Amino-N-(2-hydroxyethyl)hexanamide

Base Information

Chemical Name:6-Amino-N-(2-hydroxyethyl)hexanamide
CAS No.:35408-82-3
Molecular Formula:C8H18N2O2
Molecular Weight:174.243
Hs Code.:
DSSTox Substance ID:DTXSID60655671
Wikidata:Q82569885
Mol file:35408-82-3.mol

Synonyms:6-AMINO-N-(2-HYDROXYETHYL)HEXANAMIDE;35408-82-3;Hexanamide, 6-amino-N-(2-hydroxyethyl)-;DTXSID60655671;A1-05748

Suppliers and Price of 6-Amino-N-(2-hydroxyethyl)hexanamide

Supply Marketing:

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

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Chemical Property of 6-Amino-N-(2-hydroxyethyl)hexanamide

Chemical Property:

XLogP3:-1.1
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:7
Exact Mass:174.136827821
Heavy Atom Count:12
Complexity:118

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C(CCC(=O)NCCO)CCN

Technology Process of 6-Amino-N-(2-hydroxyethyl)hexanamide

There total 1 articles about 6-Amino-N-(2-hydroxyethyl)hexanamide 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:

: 6404-29-1
6-(tert-butoxycarbonylamino)hexanoic acid

: 35408-82-3
6-Amino-N-(2-hydroxyethyl)-capronamid

Guidance literature:: Multi-step reaction with 2 steps

1: 1) N-methylmorpholine, iBuOCOCl / 1) THF, below -15 deg C, 2) THF, -20 deg C to -15 deg C, 30 min, r.t., 1 h

2: aq. HCl / dioxane / 0.5 h / Ambient temperature

With 4-methyl-morpholine; hydrogenchloride; isobutyl chloroformate; In 1,4-dioxane;

Reference yield: 39.0%

: 35408-82-3
6-Amino-N-(2-hydroxyethyl)-capronamid

: 72155-48-7
(3S,4S)-4-tert-butoxycarbonylamino-3-hydroxy-5-phenylpentanoic acid

: 221310-31-2
{(1S,2S)-1-Benzyl-2-hydroxy-3-[5-(2-hydroxy-ethylcarbamoyl)-pentylcarbamoyl]-propyl}-carbamic acid tert-butyl ester

Guidance literature:: With benzotriazol-1-ol; dicyclohexyl-carbodiimide; In dichloromethane; 1) 0 deg C, 2) r.t., overnight;

Reference yield:

: 35408-82-3
6-Amino-N-(2-hydroxyethyl)-capronamid

: 6-((3S,4S)-4-Amino-3-hydroxy-5-phenyl-pentanoylamino)-hexanoic acid (2-hydroxy-ethyl)-amide

Guidance literature:: Multi-step reaction with 2 steps

1: 39 percent / HOBt, DCCI / CH₂Cl₂ / 1) 0 deg C, 2) r.t., overnight

2: aq. HCl / dioxane / 0.5 h / Ambient temperature

With hydrogenchloride; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In 1,4-dioxane; dichloromethane;