Cas 3380-53-8,Acetic acid 5-chloro-2-(4-chloro-phenoxy)-phenyl ester

3380-53-8

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Basic information

Product Name: Acetic acid 5-chloro-2-(4-chloro-phenoxy)-phenyl ester
Synonyms: Acetic acid 5-chloro-2-(4-chloro-phenoxy)-phenyl ester
CAS NO:3380-53-8
Molecular Formula:
Molecular Weight: 297.138
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Acetic acid 5-chloro-2-(4-chloro-phenoxy)-phenyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid 5-chloro-2-(4-chloro-phenoxy)-phenyl ester(3380-53-8)
EPA Substance Registry System: Acetic acid 5-chloro-2-(4-chloro-phenoxy)-phenyl ester(3380-53-8)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 3380-53-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 3380-53-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,8 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3380-53:
(6*3)+(5*3)+(4*8)+(3*0)+(2*5)+(1*3)=78
78 % 10 = 8
So 3380-53-8 is a valid CAS Registry Number.

3380-53-8Upstream product

129643-72-7 1-(5-chloro-2-(4-chlorophenoxy)phenyl)ethanone

3380-53-8Downstream Products

3380-30-1 5-chloro-2-(4-chlorophenoxy)phenol

3380-53-8Relevant academic research and scientific papers

Method for preparing diclosan through Baeyer-Villiger oxidation

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Paragraph 0010; 0032; 0010; 0037-0051, (2021/07/01)

The invention provides a method for preparing diclosan by using urea peroxide as an oxidizing agent. Particularly, the method comprises the following steps: (1) oxidizing 5-chloro-2-(4-chloro-phenoxy)-acetophenone in an inert solvent by using urea peroxide as an oxidizing agent to obtain an intermediate I; and (2) hydrolyzing the intermediate I to obtain the diclosan. The method is safe in production process, mild in reaction and suitable for industrial production.

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