6-Methoxy-1,2,3,4-tetrahydro-naphthalen-1-ylamine hydrochloride

Base Information

• Chemical Name: 6-Methoxy-1,2,3,4-tetrahydro-naphthalen-1-ylamine hydrochloride
• CAS No.: 39226-88-5
• Molecular Formula: C₁₁H₁₅NO*ClH
• Molecular Weight: 213.707
• Hs Code.: 2922299090
• DSSTox Substance ID: DTXSID10959999
• Mol file: 39226-88-5.mol

Synonyms:39226-88-5;6-METHOXY-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-YLAMINE HYDROCHLORIDE;6-methoxy-1,2,3,4-tetrahydronaphthalen-1-amine hydrochloride;(6-METHOXY-1,2,3,4-TETRAHYDRO-1-NAPHTHALENYL)AMINE HYDROCHLORIDE;6-methoxy-1,2,3,4-tetrahydronaphthalen-1-amine;hydrochloride;SCHEMBL10357354;DTXSID10959999;MFCD01712013;AKOS004107388;AB09820;SB79402;BS-37553;N12359;6-METHOXY-1,2,3,4-TETRA HYDRO-NAPHTHALEN-1-YLAMINE HCL;6-Methoxy-1,2,3,4-tetrahydronaphthalen-1-amine--hydrogen chloride (1/1)

Chemical Property of 6-Methoxy-1,2,3,4-tetrahydro-naphthalen-1-ylamine hydrochloride

Chemical Property:

• Vapor Pressure: 0.00109mmHg at 25°C
• Boiling Point: 300.9°Cat760mmHg
• Flash Point: 140.8°C
• PSA: 35.25000
• Density: g/cm³
• LogP: 3.53360
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 213.0920418
• Heavy Atom Count: 14
• Complexity: 172

Purity/Quality:

98%min ^*data from raw suppliers

6-Methoxy-1,2,3,4-tetrahydro-naphthalen-1-ylamineHydrochloride ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC2=C(C=C1)C(CCC2)N.Cl

Technology Process of 6-Methoxy-1,2,3,4-tetrahydro-naphthalen-1-ylamine hydrochloride

There total 6 articles about 6-Methoxy-1,2,3,4-tetrahydro-naphthalen-1-ylamine 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: 79.0%

→ 6-methoxy-1,2,3,4-tetrahydronaphthalene-1-ylamine hydrochloride (39226-88-5,911372-77-5,911372-79-7)

Guidance literature:

Reference yield:

6-methoxy-1-tetralone oxime (54951-36-9) → 6-methoxy-1,2,3,4-tetrahydronaphthalene-1-ylamine hydrochloride (39226-88-5,911372-77-5,911372-79-7)

Guidance literature:

With hydrogenchloride; hydrogen; palladium 10% on activated carbon; In ethanol; water; under 760.051 Torr;

Reference yield:

6-methoxy-1-amino-1,2,3,4-tetrahydronaphthalene (52373-02-1,314019-11-9) → 6-methoxy-1,2,3,4-tetrahydronaphthalene-1-ylamine hydrochloride (39226-88-5,911372-77-5,911372-79-7)

Guidance literature:

With hydrogenchloride; In diethyl ether; at 0 ℃; for 0.5h;

DOI:10.1055/s-1988-27747

upstream raw materials:

6-methoxy-1-amino-1,2,3,4-tetrahydronaphthalene

6-methoxy-1,2,3,4-tetrahydronaphthalene

1-azido-6-methoxy-1,2,3,4-tetrahydronaphthalene

6-methoxy-1-tetralone oxime

Refernces

• 1、 -. "N6-SUBSTITUTED ADENOSINE DERIVATIVES AND N6-SUBSTITUTED ADENINE DERIVATIVES AND USES THEREOF". Paragraph 0383. . Retrieved 2013/03/26.
• 2、 -. "Substituted amino-5,6,7,8-tetrahydronaphthyl-oxyacetic acids, processes for their preparation and their use as medicaments". . . Retrieved 2008/06/13.