60452-44-0 Usage
General Description
2-(Dimethylamino)ethyl (-)-(1-hydroxycyclopentyl)phenylacetate hydrochloride is a chemical compound that belongs to the class of phenylacetic acids. It is a hydrochloride salt and its molecular formula is C18H27NO3Cl. 2-(Dimethylamino)ethyl (-)-(1-hydroxycyclopentyl)phenylacetate hydrochloride is often used in pharmaceutical research and development as a potential drug candidate for treating various medical conditions. Its chemical structure contains a cyclopentyl ring and an ethyl group that are substituted by a dimethylamino group and a phenylacetic acid moiety. The hydrochloride salt form of 2-(Dimethylamino)ethyl (-)-(1-hydroxycyclopentyl)phenylacetate hydrochloride helps to make it more stable and soluble in aqueous solutions, which is important for its pharmaceutical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 60452-44-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,5 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60452-44:
(7*6)+(6*0)+(5*4)+(4*5)+(3*2)+(2*4)+(1*4)=100
100 % 10 = 0
So 60452-44-0 is a valid CAS Registry Number.
60452-44-0Relevant academic research and scientific papers
Preparation method of cyclopentolate hydrochloride
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Paragraph 0014; 0041, (2017/05/04)
The invention relates to a preparation method of an M-type cholinoceptor blocker cyclopentolate hydrochloride. The preparation method comprises that phenylacetic acid as an initial raw material and cyclopentanone undergoes a reaction to produce 2-(1-hydroxycyclopentyl)-phenylacetic acid (as intermediate 3), the 2-(1-hydroxycyclopentyl)-phenylacetic acid undergoes a replacement reaction and the reaction product undergoes a salification reaction to produce cyclopentolate hydrochloride. The preparation method can be operated simply, is safe and controllable, has low labor protection demands and is suitable for industrial production.