6-AMINO-1,2,3,4-TETRAHYDRO-ISOQUINOLIN HYDROCHLORIDE

Base Information

• Chemical Name: 6-AMINO-1,2,3,4-TETRAHYDRO-ISOQUINOLIN HYDROCHLORIDE
• CAS No.: 175871-42-8
• Molecular Formula: C₉H₁₂N₂*2ClH
• Molecular Weight: 221.13
• Hs Code.: 2933499090
• Mol file: 175871-42-8.mol

Synonyms:6-Isoquinolinamine,1,2,3,4-tetrahydro-, monohydrochloride (9CI); 6-Amino-1,2,3,4-tetrahydroisoquinolinehydrochloride

Chemical Property of 6-AMINO-1,2,3,4-TETRAHYDRO-ISOQUINOLIN HYDROCHLORIDE

Chemical Property:

• Vapor Pressure: 4.59E-05mmHg at 25°C
• Boiling Point: 344.7°Cat760mmHg
• Flash Point: 162.3°C
• PSA: 38.05000
• Density: g/cm³
• LogP: 2.62650

Purity/Quality:

97% ^*data from raw suppliers

6-Amino-1,2,3,4-tetrahydroisoquinolineHydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Uses: 6-Amino-1,2,3,4-tetrahydroisoquinoline is used as a reactant in the preparation of iodine-125-labeled iodotetrahydroisoquioline. 6-Amino-1,2,3,4-tetrahydroisoquinoline is also used as a reactant for the preparation of imidazo-thiazoles as multitargeted inhibitors of IGF receptor.

Technology Process of 6-AMINO-1,2,3,4-TETRAHYDRO-ISOQUINOLIN HYDROCHLORIDE

There total 2 articles about 6-AMINO-1,2,3,4-TETRAHYDRO-ISOQUINOLIN 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:

tert-butyl 6-amino-3,4-dihydroisoquinoline-2(1H)-carboxylate (164148-92-9) → 1,2,3,4-tetrahydroisoquinolin-6-amine bishydrochloride (175871-42-8)

Guidance literature:

With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 15h;

Reference yield:

isoquinolin-1-ylamine (1532-84-9) → 1,2,3,4-tetrahydroisoquinoline-6-amine monohydrochloride (175871-42-8)

Guidance literature:

With hydrogenchloride; hydrogen; acetic acid; In methanol; ethanol; dichloromethane; chloroform;

upstream raw materials:

isoquinolin-1-ylamine

tert-butyl 6-amino-3,4-dihydroisoquinoline-2(1H)-carboxylate

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