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74894-65-8

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74894-65-8 Usage

General Description

1-(3-chloro-4-fluorophenyl)-3-(ethoxymethylidene)pyrrolidine-2,5-dione is a chemical compound that is used in scientific research and drug development. It has a pyrrolidine-2,5-dione core with a 3-chloro-4-fluorophenyl group and an ethoxymethylidene substituent. The compound may have potential pharmaceutical applications due to its structure and properties. It is likely to be a part of the ongoing research and development of new drugs and medical treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 74894-65-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,8,9 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74894-65:
(7*7)+(6*4)+(5*8)+(4*9)+(3*4)+(2*6)+(1*5)=178
178 % 10 = 8
So 74894-65-8 is a valid CAS Registry Number.

74894-65-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (3E)-1-(3-chloro-4-fluorophenyl)-3-(ethoxymethylidene)pyrrolidine-2,5-dione

1.2 Other means of identification

Product number -
Other names -

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:74894-65-8 SDS

74894-65-8Downstream Products

74894-65-8Relevant articles and documents

PYRIDINIUM p-TOLUENESULFONYLMETHYLIDE AS A FORMYL ANION EQUIVALENT

Abramovitch, Rudolph A.,Mathur, Suchet S.,Saunders, Daniel W.,Vanderpool, Danny P.

, p. 705 - 708 (2007/10/02)

Pyridinium p-toluenesulfonylmethylide serves as a formyl anion equivalent and, in the presence of an alcohol, undergoes 1,4-addition to N-substituted maleimides to give alkoxy- (or aryloxy)-methylene-succinimides.The protected aldehyde group can be libera

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