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(7-Methoxy-1-naphthyl)acetic acid chloride is a chemical compound with the molecular formula C12H11ClO3. It is derived from (7-methoxy-1-naphthyl)acetic acid, where the hydroxyl group is replaced by a chlorine atom, forming an acyl chloride. (7-methoxy-1-naphthyl)acetic acid chloride is a white to off-white crystalline solid and is soluble in organic solvents such as dichloromethane and ethyl acetate. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the preparation of compounds with potential anti-inflammatory, analgesic, and antipyretic properties. Due to its reactivity, it is important to handle (7-methoxy-1-naphthyl)acetic acid chloride with care, typically under an inert atmosphere and using appropriate protective equipment.

6836-23-3

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6836-23-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6836-23-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,3 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6836-23:
(6*6)+(5*8)+(4*3)+(3*6)+(2*2)+(1*3)=113
113 % 10 = 3
So 6836-23-3 is a valid CAS Registry Number.

6836-23-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(7-methoxynaphthalen-1-yl)acetyl chloride

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6836-23-3 SDS

6836-23-3Relevant academic research and scientific papers

PROCESS FOR PREPARATION OF AGOMELATINE AND CRYSTALLINE FORM I THEREOF

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Page/Page column 16, (2014/01/17)

An improved process for the preparation of agomelatine of formula (I) and a new process for the preparation of crystalline form I of agomelatine are provided.

HETEROCYCLIC COMPOUNDS AND METHODS OF USE THEREOF

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Paragraph 00360, (2014/07/21)

Provided herein are heterocyclyl compounds, methods of their synthesis, pharmaceutical compositions comprising the compounds, and methods of their use. The compounds provided herein are useful for the treatment, prevention, and/or management of various neurological disorders, including but not limited to, psychosis and schizophrenia.

AGOMELATINE AND PHARMACEUTICAL COMPOSITIONS THEREOF

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Page/Page column 8, (2012/07/27)

Agomelatine crystal, which is a drug for treating depression, and pharmaceutical compositions thereof are provided. The X-ray powder diffraction spectra of such agomelatine crystal, which is irradiated by Cu-Kα and showed by 20(degree), has characteristic diffraction peaks at 12.84, 13.84, 16.14, 18.56, 19.12, 20.86, 21.20, 23.84; its IR absorption pattern has characteristic absorption peaks at about 3234, 3060, 2940, 1638, 1511, 1436, 1249, 1215, 1184, 1032, 908, 828, 755, 588 cm-1; and its DSC endothermic transition temperature is 97.6°C. The use of the agomelatine crystal as an active ingredient in preparing a medicament for the treatment of depression is also provided.

SUBSTITUTED NAPHTHALENES

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Page/Page column 35, (2008/12/08)

Disclosed herein are substituted naphthalene-based melatonin (MT) receptor modulators and/or 5-HT receptor modulators of Formula I, process of preparation thereof, pharmaceutical compositions thereof, and methods of use thereof.

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