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27507-54-6

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27507-54-6 Usage

Type of compound

Isoindole-1,3-dione derivative

Structure

Dimer with two isoindole-1,3-dione units linked by an oxygen atom

Contains

Two methyl groups

Industrial and research applications

Exhibits properties suitable for various uses

Precautions

May pose health and environmental hazards if not properly managed

Further research

Necessary to fully understand its characteristics and potential uses

Check Digit Verification of cas no

The CAS Registry Mumber 27507-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,5,0 and 7 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 27507-54:
(7*2)+(6*7)+(5*5)+(4*0)+(3*7)+(2*5)+(1*4)=116
116 % 10 = 6
So 27507-54-6 is a valid CAS Registry Number.

27507-54-6SDS

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 4.4-oxybis(N-methylphthalimide)

1.2 Other means of identification

Product number -
Other names 1H-ISOINDOLE-1,3(2H)-DIONE, 5,5'-OXYBIS[2-METHYL-

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:27507-54-6 SDS

27507-54-6Downstream Products

27507-54-6Relevant articles and documents

Diaryl Ether Formation via Nitro Displacement with 4-Methylphenol and Potassium Carbonate on 4-Nitro-N-methylphthalimide

Relles, Howard M.,Johnson, Donald S.,Dellacoletta, B. A.

, p. 1374 - 1379 (1980)

Conditions for the equilibration between a nitro-substituted imide and its ring-opened amide-acid salt were established.Evidence was found that nitro displacement by an aryl oxide nucleophile occured only in the imide form.Extensive 13C NMR data are presented as structural evidence and for distinguishing amide acid isomers.

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