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1260895-08-6

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1260895-08-6 Usage

Description

(1-benzhydryl-2-methylazetidin-3-yl)methanamine, also known as benzatropine, is a synthetic anticholinergic drug primarily used in the treatment of Parkinson's disease. It functions by blocking the action of acetylcholine, a neurotransmitter involved in movement control, thereby reducing the symptoms of tremors, stiffness, and slowness of movement associated with Parkinson's disease.

Uses

Used in Pharmaceutical Industry:
(1-benzhydryl-2-methylazetidin-3-yl)methanamine is used as an adjunct therapy for the treatment of Parkinson's disease to alleviate symptoms such as tremors, stiffness, and slowness of movement. Its mechanism of action involves blocking acetylcholine, leading to a reduction in these symptoms and improving the patient's quality of life.
However, it is important to note that benzatropine may have potential side effects, including dry mouth, constipation, and blurred vision. Therefore, it should be used cautiously in individuals with certain medical conditions such as glaucoma.

Check Digit Verification of cas no

The CAS Registry Mumber 1260895-08-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,8,9 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1260895-08:
(9*1)+(8*2)+(7*6)+(6*0)+(5*8)+(4*9)+(3*5)+(2*0)+(1*8)=166
166 % 10 = 6
So 1260895-08-6 is a valid CAS Registry Number.

1260895-08-6Downstream Products

1260895-08-6Relevant articles and documents

7-Azetidinylquinolones as antibacterial agents. 2. Synthesis and biological activity of 7-(2,3-disubstituted-1-azetidinyl)-4-oxoquinoline- and -1,8-naphthyridine-3-carboxylic acids. Properties and structure-activity relationships of quinolones with an aze

Frigola,Torrens,Castrillo,Mas,Vano,Berrocal,Calvet,Salgado,Redondo,Garcia-Granda,Valenti,Quintana

, p. 4195 - 4210 (2007/10/02)

A series of 7-(2,3-disubstituted-1-azetidinyl)-1,4-dihydro-6-fluoro-4- oxoquinoline- and -1,8-naphthyridine-3-carboxylic acids, with varied substituents at the 1-, 5-, and 8-positions, was prepared to study the effects on potency and physicochemical prope

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