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43113-25-3

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43113-25-3 Usage

Type of compound

bis-dioxopiperazine

Common uses

crosslinking agent in the production of polymeric materials

Known for

high thermal stability, used in the manufacture of polymers, resins, and adhesives

Potential applications

biomedical and pharmaceutical fields, particularly in drug delivery systems and tissue engineering

Unique features

versatile and valuable chemical in various industries due to its structure and properties

Check Digit Verification of cas no

The CAS Registry Mumber 43113-25-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,3,1,1 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 43113-25:
(7*4)+(6*3)+(5*1)+(4*1)+(3*3)+(2*2)+(1*5)=73
73 % 10 = 3
So 43113-25-3 is a valid CAS Registry Number.

43113-25-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-[2-(1,3-dioxoisoindol-2-yl)ethoxy]ethyl]isoindole-1,3-dione

1.2 Other means of identification

Product number -
Other names 3-oxapentane-1,5-diphthalimide

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:43113-25-3 SDS

43113-25-3Upstream product

43113-25-3Relevant articles and documents

PECULIARITIES OF THE REACTION OF N,N'-SUBSTITUTED DIPHTHALIMIDES WITH AMINES

Anikin, V. F.,Ganin, E. V.,Rozynov, B. V.,Zakharova, R. M.,Kamalov, G. L.

, p. 193 - 196 (2007/10/02)

Macrocyclic phthalic acid diamides were obtained by the reaction of N,N'-substituted diphthalimides with polyoxyethylenediamines, while the corresponding tetraamides were obtained with primary aliphatic amines.It is shown that the reaction is a thermodynamically controlled process.

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