52413-42-0 Usage
Chemical structure
Indazole derivative with a benzyl group and a dimethylamino propyl group
Potential applications
Pharmaceutical research and drug development
Safety precautions
Handle with care and follow proper safety protocols in a laboratory setting
Biological activities
Not specified in the material provided, but may be inferred due to its potential applications in pharmaceutical research and drug development
Structural properties
Not explicitly detailed in the material, but can be inferred from the molecular formula and chemical structure
Chemical class
Indazole derivative
Functional groups
Benzyl group, dimethylamino propyl group
Physical state
Not specified in the material, but likely a solid or liquid at room temperature based on typical properties of organic compounds with similar structures
Solubility
Not specified in the material, but may be inferred based on the presence of polar functional groups (e.g., dimethylamino) which could suggest some level of solubility in polar solvents like water or alcohols
Check Digit Verification of cas no
The CAS Registry Mumber 52413-42-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,4,1 and 3 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52413-42:
(7*5)+(6*2)+(5*4)+(4*1)+(3*3)+(2*4)+(1*2)=90
90 % 10 = 0
So 52413-42-0 is a valid CAS Registry Number.
52413-42-0Relevant articles and documents
Photodegradation of benzydamine: Phototoxicity of an isolated photoproduct on erythrocytes
Vargas,Rivas,Machado,Sarabia
, p. 371 - 372 (1993)
Benzydamine hydrochloride (Tantum, 1) is a photoallergic and phototoxic anti-inflammatory and analgesic agent. This drug is photolabile under aerobic and anaerobic conditions. Irradiation of a methanol solution of benzydamine under oxygen or argon at 300 nm affords 5-hydroxybenzydamine (2) and 2-β- dimethylaminopropyl-1-benzylindalolin-3-one (3) as the main isolated and spectroscopically identified photoproducts. A radical intermediate was evidenced by thiobarbituric acid that was used as a radical sonde, as well as by the dimerization of cysteine. Erythrocyte lysis phososensitized by 1, 2, and 3 was investigated.
