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2752-87-6

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2752-87-6 Usage

Type of compound

Ketone derivative

Functional groups

Dimethylamino group, Naphthalenyl ring

Usage

Organic synthesis, reagent in analytical chemistry, fluorescent dye, organic semiconductors, pharmaceuticals, agrochemicals, specialty chemicals

Potential applications

Sensor technologies, organic light-emitting diodes (OLEDs), advanced materials

Unique properties

Electronic and optical properties

Check Digit Verification of cas no

The CAS Registry Mumber 2752-87-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,5 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2752-87:
(6*2)+(5*7)+(4*5)+(3*2)+(2*8)+(1*7)=96
96 % 10 = 6
So 2752-87-6 is a valid CAS Registry Number.

2752-87-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(dimethylamino)-1-naphthalen-2-ylpropan-1-one

1.2 Other means of identification

Product number -
Other names 3-(Dimethylamino)-1-(2-naphthyl)-1-propanone

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:2752-87-6 SDS

2752-87-6Relevant articles and documents

A method of high-efficiency production of beda quinoline

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Paragraph 0039; 0042; 0045; 0047-0049; 0051; 0054; 0057, (2017/09/26)

The invention relates to a method for high efficiency production of Bedaquiline. The method comprises that through optical resolution of 1-(6-bromo-2-methoxy-3-quinolyl)-4-dimethylamino-2-(1-naphthyl)-1-phenyl-2-butanol, Bedaquiline and other isomers are obtained, the other isomers undergo a reaction under the action of an alkali to produce key intermediate compounds A and B, and the key intermediate compounds A and B are separated and undergo a reaction to produce Bedaquiline. The method realizes high efficiency production of Bedaquiline, prevents large waste of materials, saves a cost and is suitable for large scale industrial production.

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