74894-65-8 Usage
Chemical structure
The compound has a pyrrolidine-2,5-dione core with a 3-chloro-4-fluorophenyl group and an ethoxymethylidene substituent.
Application
It is used in scientific research and drug development.
Potential pharmaceutical applications
Due to its structure and properties, the compound may have potential pharmaceutical applications.
Ongoing research and development
It is likely to be a part of the ongoing research and development of new drugs and medical treatments.
Molecular weight
The molecular weight of the compound is approximately 270.67 g/mol.
Appearance
The compound is likely to be a solid, based on its molecular weight and structure.
Solubility
The compound's solubility is not explicitly mentioned, but it may be soluble in organic solvents such as ethanol, methanol, or dimethyl sulfoxide (DMSO) due to its structure.
Stability
The stability of the compound is not explicitly mentioned, but it may be sensitive to light, heat, or moisture, as is common with many pharmaceutical compounds.
Safety precautions
As with any chemical compound, appropriate safety precautions should be taken when handling and storing 1-(3-chloro-4-fluorophenyl)-3-(ethoxymethylidene)pyrrolidine-2,5-dione, including the use of personal protective equipment (PPE) and proper disposal methods.
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.
74894-65-8Relevant academic research and scientific papers
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
