6-AMINOCAPRONIC ACID ETHYL ESTER HYDROCHLORIDE

Base Information

• Chemical Name: 6-AMINOCAPRONIC ACID ETHYL ESTER HYDROCHLORIDE
• CAS No.: 3633-17-8
• Molecular Formula: C8H17 N O2 . Cl H
• Molecular Weight: 195.689
• Hs Code.: 2922499990
• Mol file: 3633-17-8.mol

Synonyms:Hexanoicacid, 6-amino-, ethyl ester, hydrochloride (7CI,8CI,9CI); 6-Aminocaproic acidethyl ester hydrochloride; 6-Aminohexanoic acid ethyl ester hydrochloride;Ethyl 6-amininohexanoate hydrochloride; Ethyl 6-aminocaproate hydrochloride;Ethyl 6-aminohexanoate hydrochloride; Ethyl e-aminocaproatehydrochloride

Chemical Property of 6-AMINOCAPRONIC ACID ETHYL ESTER HYDROCHLORIDE

Chemical Property:

• Boiling Point: 211.4°Cat760mmHg
• Flash Point: 80.7°C
• PSA: 52.32000
• Density: 0.949g/cm³
• LogP: 2.57090
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C

Purity/Quality:

98%,99%, ^*data from raw suppliers

ethyl6-aminohexanoatehydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 6-AMINOCAPRONIC ACID ETHYL ESTER HYDROCHLORIDE

There total 5 articles about 6-AMINOCAPRONIC ACID ETHYL ESTER HYDROCHLORIDE 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: 100.0%

6-aminohexanoic acid (60-32-2,93208-38-9) → ethyl 6-aminocaproate hydrochloride (3633-17-8)

Guidance literature:

Reference yield: 97.0%

ethanol (64-17-5) + 6-aminohexanoic acid (60-32-2,93208-38-9) → ethyl 6-aminocaproate hydrochloride (3633-17-8)

Guidance literature:

With thionyl chloride; at 0 - 20 ℃; for 12.5h;

Reference yield: 90.0%

7-ethoxy-2H 3,4,5,6-tetrahydroazepinium hydrochloride (94704-41-3) → ethyl 6-aminocaproate hydrochloride (3633-17-8)

Guidance literature:

With water; for 24h; Ambient temperature;

upstream raw materials:

7-ethoxy-2H 3,4,5,6-tetrahydroazepinium hydrochloride

ethanol

6-aminohexanoic acid

caprolactam

Downstream raw materials:

ethyl 6-(1,3-dibenzylhexahydro-2-oxo-1,3,5-triazin-5-yl)hexanoate

N-(5-ethoxycarbonylpentyl)-2-nitro-3-benzyloxy-4-methylbenzamide

N--2-oxoethyl)-DL-homocysteinyl>-N-(5-ethoxycarbonylpentyl)glycinamide

6-{[1-(5-Phenyl-isoxazol-3-yl)-meth-(Z)-ylidene]-amino}-hexanoic acid ethyl ester

Refernces

• 1、 Goh, Jeffrey,Loh, Teck-Peng,Maraswami, Manikantha. "Macrolactam Synthesis via Ring-Closing Alkene-Alkene Cross-Coupling Reactions". supporting information. p. 9724 - 9728. Retrieved 2020/12/21.
• 2、 Dashko, L. V.,Dmitriev, D. V.,Pestov, S. M.,Flid, V. R.. "Cross aldol condensation of acetaldehyde and formaldehyde in the presence of bifunctional systems". . p. 1732 - 1737. Retrieved 2015/02/05.