77008-58-3 Usage
General Description
The chemical compound (2-CHLOROPHENYL)(3-CHLOROPHENYL)METHANONE, also known as 2,5-dichloroacetophenone, is a white to light yellow crystalline powder with a molecular formula C14H9Cl3O. It is a ketone derivative and is commonly used in the synthesis of pharmaceuticals and other organic compounds. This chemical is often employed as an intermediate in the production of various drugs and can also be utilized as a flavoring agent in the food industry. Additionally, it has potential applications in research and development, particularly in the field of organic chemistry. As with all chemicals, proper handling and storage procedures should be followed to ensure safety.
Check Digit Verification of cas no
The CAS Registry Mumber 77008-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,0,0 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77008-58:
(7*7)+(6*7)+(5*0)+(4*0)+(3*8)+(2*5)+(1*8)=133
133 % 10 = 3
So 77008-58-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H8Cl2O/c14-10-5-3-4-9(8-10)13(16)11-6-1-2-7-12(11)15/h1-8H
77008-58-3Relevant articles and documents
POTENTIAL ANTICONVULSANTS: 3-CHLOROBENZOPHENONE DERIVATIVES
Jilek, Jiri,Urban, Jiri,Kmonicek, Vojtech,Pomykacek, Josef,Holubek, Jiri,et al.
, p. 2248 - 2260 (2007/10/02)
Reactions of 2-(2-iodoacetamido)-5-chlorobenzophenone with 2-amino-2-phenylethanol, 2-amino-1-phenylethanol, 3-amino-2-phenylpropanol, D(+)-norpseudoephedrine, and 2-aminopropane-2-carbonitrile gave the 2-substituted N-(2-benzoyl-4-chlorophenyl)acetamides X-XIV. 2,3'-Dichlorobenzhydrol (XVI) and 2,3'-dichlorobenzhydryl chloride (XIX) were transformed to the ethers XVII and XVIII and to the amines XXI-XXIV.Compound XVI was oxidized to the ketone XXV which was transformed via the oxime XXVI to compound XXVII.The basic products were converted to salts which were pharmacologically tested.Compounds X, XVII, XXIII, and XXVII showed anticonvulsant effects and some other neurotropic activities.
