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75810-50-3

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75810-50-3 Usage

Chemical structure

2-(4-Methoxyphenyl)-1-methyl-5-oxo-3-pyrrolidinecarboxylic acid

Primary uses

Epilepsy, neuropathic pain, restless legs syndrome

Off-label uses

Anxiety, bipolar disorder, alcohol withdrawal symptoms

Classification

Anticonvulsant or anti-epileptic drug

Mechanism of action

Affects chemicals and nerves in the body involved in seizures and some types of pain

Available forms

Tablets, capsules, oral solutions

Tolerance

Generally well-tolerated

Side effects

Dizziness, drowsiness, and potential for dependence

Precautions

Use with caution when operating heavy machinery or driving due to potential for dizziness and drowsiness

Check Digit Verification of cas no

The CAS Registry Mumber 75810-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,1 and 0 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 75810-50:
(7*7)+(6*5)+(5*8)+(4*1)+(3*0)+(2*5)+(1*0)=133
133 % 10 = 3
So 75810-50-3 is a valid CAS Registry Number.

75810-50-3Upstream product

75810-50-3Downstream Products

75810-50-3Relevant articles and documents

Toward lead-oriented synthesis: One-pot version of castagnoli condensation with nonactivated alicyclic anhydrides

Ryabukhin, Sergey V.,Panov, Dmitriy M.,Granat, Dmitry S.,Ostapchuk, Eugeniy N.,Kryvoruchko, Dmitriy V.,Grygorenko, Oleksandr O.

, p. 146 - 153 (2014/04/03)

One-pot variation of Castagnoli condensation, that is, reaction of cyclic anhydrides, amines, and aldehydes, has been developed as a combinatorial approach to 1,2-disubstituted 5-oxopyrrolidine- and 6-oxopiperidine-3-carboxylic acids, as well as their benzo-analogues. Utility of the method to multigram preparation of building blocks and synthetic intermediates was also demonstrated. The final products are obtained in high yields and diastereoselectivity. The method fits well in the concept of lead-oriented synthesis; in particular, it can be used for the design of lead-like compound libraries, even if the strictest cut-offs are applied to the physicochemical properties of their members.

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