60573-65-1 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
This describes the specific arrangement of atoms and functional groups in the compound.
Explanation
The physical appearance of the compound, which is a white to off-white crystalline powder.
Explanation
The compound's solubility properties, indicating that it does not dissolve in water but does dissolve in organic solvents.
Explanation
The primary industries in which the compound is used, which are the pharmaceutical and chemical industries.
Explanation
The compound is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals.
Explanation
The compound has potential applications in materials science and organic synthesis, indicating its versatility in different fields.
Explanation
The compound is known to exhibit various pharmacological properties, making it a valuable building block for the development of novel drug molecules.
Explanation
The compound is a brominated derivative, meaning it has a bromine atom added to the isobenzofuranone structure.
Structure
1(3H)-Isobenzofuranone, 6-bromo-3,3-diphenyl-
Appearance
White to off-white crystalline powder
Solubility
Insoluble in water, soluble in organic solvents
Industry Applications
Pharmaceutical and chemical industries
Usage
Intermediate in the synthesis of pharmaceuticals and agrochemicals
Potential Applications
Materials science and organic synthesis
Pharmacological Properties
Exhibits a range of pharmacological properties
Derivative
Brominated derivative of isobenzofuranone
Check Digit Verification of cas no
The CAS Registry Mumber 60573-65-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,5,7 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 60573-65:
(7*6)+(6*0)+(5*5)+(4*7)+(3*3)+(2*6)+(1*5)=121
121 % 10 = 1
So 60573-65-1 is a valid CAS Registry Number.
60573-65-1Relevant articles and documents
Facile synthesis of phthalides from methyl ortho-iodobenzoates and ketones via an iodinemagnesium exchange reaction using a silylmethyl Grignard reagent
Nakamura, Yu,Yoshida, Suguru,Hosoya, Takamitsu
, p. 858 - 861 (2017/06/13)
Phthalides have been easily prepared by the treatment of methyl o-iodobenzoates with a silylmethyl Grignard reagent in the presence of ketones. The electron-withdrawing ester moiety of methyl o-iodobenzoates and the low nucleophilicity of the silylmethyl Grignard reagent prompted a smooth iodinemagnesium exchange reaction, at room temperature, without affecting the ester moiety or resulting in an undesired reaction with electrophilic ketones. This simple method, wherein special control of the reaction temperature was unnecessary, has allowed the synthesis of various phthalides, including a phenolphthalein derivative.
