2-(7-Methoxy-1-naphthyl)ethylamine hydrochloride | CAS:139525-77-2

2-(7-Methoxy-1-naphthyl)ethylamine hydrochloride

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2-(7-Methoxy-1-naphthyl)ethylamine hydrochloride Description

Source:
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage:	Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C). Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving:	The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.

Structure Identification:

SI20050030417T on 11 Feb 2005.

Novel process for synthesizing and a novel crystal form of agomelatin as well as pharmaceutical preparations containing these.[Reference: WebLink]

METHODS AND RESULTS:
Producing agomelatin comprises reacting 7-methoxy-1-tetralone with cyanoacetic acid in presence of organo-ammonium carboxylate catalyst (V), contacting resulting 2-(7-methoxy-3,4-dihydro-1-naphthyl)acetonitrile (VI) with hydrogenation catalyst in presence of allylic compound to give 2-(7-methoxy-1-naphthyl)acetonitrile (VII), hydrogenating (VII) to give 2-(7-Methoxy-1-naphthyl)ethylamine hydrochloride (VIII) and acetylating. Producing agomelatin (N-(2-(7-methoxy-1-naphthyl)ethyl)acetamide) comprises: (i) reacting 7-methoxy-1-tetralone with cyanoacetic acid in the presence of an organoammonium carboxylate catalyst of formula (V) while removing water; (ii) contacting the resulting 2-(7-methoxy-3,4-dihydro-1-naphthyl)acetonitrile (VI) with a hydrogenation catalyst in the presence of an allylic compound to give 2-(7-methoxy-1-naphthyl)acetonitrile (VII); (iii) hydrogenating (VII) in the presence of Raney nickel in ethanol and treating the product with hydrochloric acid to give 2-(7-Methoxy-1-naphthyl)ethylamine hydrochloride (VIII); and (iv) reacting (VIII) successively with.

Product Name	2-(7-Methoxy-1-naphthyl)ethylamine hydrochloride
Price:
CAS No.:	139525-77-2
Catalog No.:	CFN90089
Molecular Formula:	C₁₃H₁₅NO.HCl
Molecular Weight:	237.73 g/mol
Purity:	>=98%
Type of Compound:	Phenols
Physical Desc.:	Powder
Source:
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download:	COA MSDS
Similar structural:	Comparison (Web) (SDF)
Guestbook:

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Phenols Compound Library

	1 mg	5 mg	10 mg	20 mg	25 mg
1 mM	4.2065 mL	21.0323 mL	42.0645 mL	84.1291 mL	105.1613 mL
5 mM	0.8413 mL	4.2065 mL	8.4129 mL	16.8258 mL	21.0323 mL
10 mM	0.4206 mL	2.1032 mL	4.2065 mL	8.4129 mL	10.5161 mL
50 mM	0.0841 mL	0.4206 mL	0.8413 mL	1.6826 mL	2.1032 mL
100 mM	0.0421 mL	0.2103 mL	0.4206 mL	0.8413 mL	1.0516 mL

CFN90087	7-Methoxy-1-naphthaleneacetic acid ethyl ester	6836-21-1	244.29	C₁₅H₁₆O₃
CFN92248	Salpriolactone	132278-72-9	242.3	C₁₅H₁₄O₃
CFN96584	Nepodin	3785-24-8	216.24	C₁₃H₁₂O₃
CFN97101	Torachrysone 8-O-glucoside	64032-49-1	408.4	C₂₀H₂₄O₉
CFN95130	Cassiaglycoside II	2241081-56-9	556.5	C₂₅H₃₂O₁₄
CFN95131	Torosachrysone 8-O-beta-gentiobioside	94356-13-5	612.6	C₂₈H₃₆O₁₅
CFN90516	Aristolochic acid C	4849-90-5	327.25	C₁₆H₉NO₇
CFN99505	Aristolochic acid A	313-67-7	341.27	C₁₇H₁₁O₇N
CFN90517	7-Hydroxyaristolochic acid A	79185-75-4	357.3	C₁₇H₁₁NO₈
CFN90783	Aristolochic acid D	17413-38-6	357.3	C₁₇H₁₁NO₈