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1954-06-9

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1954-06-9 Usage

Structure

1H-Isoindole-1,3(2H)-dione with a methoxymethyl group at the 2-position

Type

Derivative of isoindole-1,3(2H)-dione

Use

Used in the synthesis of various organic compounds

Chemical properties

The presence of the methoxymethyl group at the 2-position of the isoindole ring imparts specific chemical properties to the compound, making it useful in different chemical reactions and processes.

Interest

Of interest to researchers and chemical manufacturers

Potential applications

Various fields such as pharmaceuticals, materials science, and organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 1954-06-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,5 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1954-06:
(6*1)+(5*9)+(4*5)+(3*4)+(2*0)+(1*6)=89
89 % 10 = 9
So 1954-06-9 is a valid CAS Registry Number.

1954-06-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(methoxymethyl)phthalimide

1.2 Other means of identification

Product number -
Other names N-methoxymethylphtalimide

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:1954-06-9 SDS

1954-06-9Downstream Products

1954-06-9Relevant articles and documents

Photolysis experiments on phosmet, an organophosphorus insecticide

Sinderhauf, Katrin,Schwack, Wolfgang

, p. 5990 - 5995 (2007/10/03)

The organophosphorus insecticide phosmet is used in plant protection as well as against parasites on animals. Phosmet showed numerous photoinduced reaction pathways, which first were studied in the presence of model environments for animal fur lipids (e.g

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