512-15-2 Usage
Originator
Cyclogyl,Schieffelin,US,1953
Uses
Different sources of media describe the Uses of 512-15-2 differently. You can refer to the following data:
1. Cyclopentolate is an effective mydriatic and cycloplegic that begins to act very quickly and
has a relatively short duration. It is used also in ophthalmoscopy for causing pre-operational
mydriasis.
2. thalidomide derivative for multiple myeloma and myelodysplastic syndromes
3. Cyclopentolate is a muscarinic antagonist. It is used in eye drops to dilate the eyes and prevent them from refocusing making the eyes more sensitive to light and may cause blurring.
Definition
ChEBI: A carboxylic ester resulting from the formal condensation of (1-hydroxycyclopentyl)(phenyl)acetic acid with N,N-dimethylethanolamine. A tertiary amine antimuscarinic with actions similar to atropine, it is used as its
ydrochloride salt to produce mydriasis (excessive dilation of the pupil) and cycloplegia (paralysis of the ciliary muscle of the eye) for opthalmic diagnostic procedures. It acts more quickly than atropine and has a shorter duration of action.
Manufacturing Process
To a well stirred suspension of 9 g of sodium phenyl acetate and 2.4 g of
magnesium turnings in 25 cc of anhydrous ether, a solution of 9.4 cc of
isopropyl bromide in 50 cc of anhydrous ether are added. The mixture is
refluxed for one hour (during which time propane is evolved) and then 5 cc of
cyclopentanone in 25 cc of anhydrous ether are added dropwise. The mixture
is then refluxed for one hour and poured over ice water containing some
hydrochloric acid. The ether solution is separated and extracted with 200 cc of
5% sodium hydroxide. The alkaline solution on acidification gives the free acid which is filtered off, dried in a desiccator and recrystallized from a mixture of
ethylene dichloride and petroleum ether.The product is 2-phenyl-2-(1-hydroxycyclopentyl)ethanoic acid, melting at 95°
to 97°C. Of this product, 4.5 g in 30 cc of dry isopropyl alcohol are refluxed
for 16 hours with 2.5 g of β-chloroethyl dimethyl amine. The solution is cooled
and filtered clear from the solid by-product. The solvent is removed under
reduced pressure on the steam bath and the residue is washed with
anhydrous ether. It is dissolved in ethyl acetate from which it crystallizes. It is
the hydrochloride of β-(dimethylamino)ethyl ester of 2-phenyl-2-(1-
hydroxycyclopentyl) ethanoic acid, melting at 134° to 136°C.
Brand name
Akpentolate (Akorn); Cyclogyl (Alcon); Pentolair (Bausch & Lomb); Pentolair (Pharmafair).
Therapeutic Function
Anticholinergic (ophthalmic)
Synthesis
Cyclopentolate, 2-(dimethylamino)ethylic ester of 1-hydroxycyclopentane-
α-phenylacetic acid (14.1.39), is synthesized by the esterification of α-(1- droxycylopentyl)
phenylacetic acid (14.1.38) using 2-dimethylaminoethylchloride, α-(1- Hydroxycyclopentyl)
phenylacetic acid (14.1.38) is synthesized by reacting the sodium salt of phenylacetic acid
with cyclopentanone in the presence of isopropylmagnesium bromide [30].
Veterinary Drugs and Treatments
Cyclopentolate is an anticholinergic agent that induces relaxation
of the sphincter of the iris and the ciliary muscles. When applied
topically to the eyes, it causes a rapid, intense cycloplegic and mydriatic
effect that is maximal in 15 – 60 minutes; recovery usually
occurs within 24 hours. The cycloplegic and mydriatic effects are
slower in onset and longer in duration in animal patients who have
darkly pigmented irises. Cyclopentolate is used mainly to produce
mydriasis and cycloplegia for diagnostic purposes.
Check Digit Verification of cas no
The CAS Registry Mumber 512-15-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,1 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 512-15:
(5*5)+(4*1)+(3*2)+(2*1)+(1*5)=42
42 % 10 = 2
So 512-15-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H25NO3/c1-18(2)12-13-21-16(19)15(14-8-4-3-5-9-14)17(20)10-6-7-11-17/h3-5,8-9,15,20H,6-7,10-13H2,1-2H3
512-15-2Relevant articles and documents
Preparation method of cyclopentolate hydrochloride
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Paragraph 0014; 0034; 0037; 0038, (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.
