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6,8-Dichloro-2-tetralone is an organic compound characterized by the presence of two chlorine atoms at the 6th and 8th positions on a tetralone molecule. It is a valuable intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure and reactivity.

113075-86-8

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113075-86-8 Usage

Uses

Used in Pharmaceutical Industry:
6,8-Dichloro-2-tetralone is used as a key reactant for the preparation of tetrahydrospiro[imidazolenaphthalenes], which are known as α-adrenergic agonists. These compounds play a crucial role in the development of medications targeting the adrenergic system, which is involved in various physiological processes, including blood pressure regulation, bronchodilation, and neurotransmission.

Check Digit Verification of cas no

The CAS Registry Mumber 113075-86-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,0,7 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 113075-86:
(8*1)+(7*1)+(6*3)+(5*0)+(4*7)+(3*5)+(2*8)+(1*6)=98
98 % 10 = 8
So 113075-86-8 is a valid CAS Registry Number.

113075-86-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,8-dichloro-3,4-dihydro-1H-naphthalen-2-one

1.2 Other means of identification

Product number -
Other names 2(1H)-Naphthalenone,6,8-dichloro-3,4-dihydro

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:113075-86-8 SDS

113075-86-8Downstream Products

113075-86-8Relevant academic research and scientific papers

Technological method for preparing halogenated-3,4-dihydro-1H-2-naphthalenone

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, (2017/07/20)

The invention relates to a technological preparation method of halogenated-3,4-dihydro-1H-2-naphthalenone as shown in a formula (I). (As shown in the description). According to the method disclosed by the invention, through a cheap raw material namely 2,4-dihalogeno-benzene carbonitrile, and an intermediate namely 2,4-dihalogeno-benzene acetic acid is synthesized, and through a reusable trifluoroacetic anhydride/acid system catalyst, a target product namely the halogenated-3,4-dihydro-1H-2-naphthalenone is synthesized. According to the method disclosed by the invention, a large quantity of catalysts such as aluminumtrichloride, and costly catalysts such as Rh, are not needed, and the reaction route can be shortened, so that a large quantity of reagents and time can be saved, and the industrial economic benefits can be greatly increased.

Benzazecine derivatives for cognitive and memory functions

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, (2008/06/13)

Benzazecinediones of the formula STR1 wherein R1 and R2 are independently hydrogen or chlorine, R3 is hydrogen, fluorine, chlorine, bromine or methoxy, R4 is hydrogen, chlorine or methoxy and R5 is hy

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