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2525-80-6

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2525-80-6 Usage

Usage

Primarily used as a chemical intermediate in the production of various industrial products.

Applications

Commonly used in the manufacturing of plastics, adhesives, and coatings.

Additional Uses

Also used in the production of pharmaceuticals and agrochemicals.

Physical State

Colorless liquid.

Odor

Strong odor.

Health Hazard

Considered hazardous to human health.

Environmental Hazard

Considered hazardous to the environment.

Exposure Risks

Can cause irritation to the skin, eyes, and respiratory system.

Safety Precautions

It is important to handle it with caution and follow safety protocols when working with it.

Check Digit Verification of cas no

The CAS Registry Mumber 2525-80-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,2 and 5 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2525-80:
(6*2)+(5*5)+(4*2)+(3*5)+(2*8)+(1*0)=76
76 % 10 = 6
So 2525-80-6 is a valid CAS Registry Number.

2525-80-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,3,4,4,5,5-octafluoro-1,6-diphenylhexane-1,6-dione

1.2 Other means of identification

Product number -
Other names 1,1,2,2,3,3,4,4-Octafluor-1,4-dibenzoyl-butan

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:2525-80-6 SDS

2525-80-6Relevant articles and documents

Reaction of perfluorocarbonyl chlorides with ethyl- and phenylmagnesium bromides

Chapurkin,Litinskii,Leont'eva,Chapurkin

, p. 1136 - 1138 (2005)

The structure of the products formed by the reactions of perfluoroadipoyl and perfluorocyclo-hexanedicarbonyl difluorides with ethyl- and phenylmagnesium bromides depends on the nature of the radical in the organomagnesium compound. 2005 Pleiades Publishing, Inc.

REDUCTION OF POLYFLUORINATED CARBONYL COMPOUNDS BY ETHOXYMAGNESIUM BROMIDE

Dormidontov, Yu. P.,Shadrina, L. P.

, p. 241 - 244 (2007/10/02)

The reduction of perfluoroalkyl phenyl ketones and diketones with ethoxymagnesium bromide takes place readily in the absence of branching at the α-carbon atom of the aliphatic radical and in the absence of a substituent or in the presence of only one orth

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