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17556-19-3

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17556-19-3 Usage

General Description

5-Chloro-2-tetralone is a chemical compound with the molecular formula C10H9ClO. It belongs to the class of organic compounds known as tetralones, which are cyclic ketones that contain a 6-membered aliphatic ring. The presence of a chlorine atom at the 5th position of the tetralone ring gives this compound its unique properties. 5-Chloro-2-tetralone is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It is also used in organic synthesis and as a building block for the preparation of various other chemical compounds. Its versatile nature and reactivity make it a valuable tool in chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 17556-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,5 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17556-19:
(7*1)+(6*7)+(5*5)+(4*5)+(3*6)+(2*1)+(1*9)=123
123 % 10 = 3
So 17556-19-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H7ClO/c10-9-3-1-2-6-4-7(11)5-8(6)9/h1-3H,4-5H2

17556-19-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-chloro-3,4-dihydro-1H-naphthalen-2-one

1.2 Other means of identification

Product number -
Other names 7-chloro-3,4-dihydronaphthalen-2(1H)-one

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:17556-19-3 SDS

17556-19-3Relevant articles and documents

A concise method for the synthesis of 2-tetralone by titanium tetrachloride-promoted cyclization of 4-aryl-2-hydroxybutanal diethyl acetal

Hon, Yung-Son,Devulapally, Rammohan

scheme or table, p. 5713 - 5715 (2009/12/09)

4-Aryl-2-hydroxybutanal diethyl acetal, prepared from the reaction of benzyl Grignard reagent and glycidaldehyde diethyl acetal, was treated with titanium tetrachloride to give 2-tetralone in good yield. This highly efficient transformation involves tande

Heteroaryl β-tetralin ureas as novel antagonists of human TRPV1

Jetter, Michele C.,Youngman, Mark A.,McNally, James J.,McDonnell, Mark E.,Zhang, Sui-Po,Dubin, Adrienne E.,Nasser, Nadia,Codd, Ellen E.,Flores, Christopher M.,Dax, Scott L.

, p. 6160 - 6163 (2008/03/18)

We report on a series of α-substituted-β-tetralin-derived and related phenethyl-based isoquinolinyl and hydroxynaphthyl ureas as potent antagonists of the human TRPV1 receptor. The synthesis and Structure-activity relationships (SAR) of the series are described.

Bicyclic amine derivatives and their use as anti-psychotic agents

-

, (2008/06/13)

This invention relates to compounds of formula (I) STR1 which are useful as modulators of D3 receptors, in particular as antipsychotic agents.

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