2025-33-4 Usage
General Description
(2-Pyrrolidin-3-yl-ethyl)-carbamic acid benzyl ester is a chemical compound with the molecular formula C17H23NO2. It is a benzyl ester derivative of carbamic acid, with a pyrrolidin-3-yl-ethyl substituent. (2-Pyrrolidin-3-yl-ethyl)-carbamic acid benzyl ester is commonly used as an intermediate in the synthesis of pharmaceutical drugs and agrochemicals. It has been studied for its potential as a cholinesterase inhibitor, making it of interest for the treatment of Alzheimer's disease and other neurodegenerative disorders. Additionally, it may have applications in organic synthesis and as a reagent in chemical reactions. The compound should be handled and used with care, as it may pose health and environmental hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 2025-33-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,2 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2025-33:
(6*2)+(5*0)+(4*2)+(3*5)+(2*3)+(1*3)=44
44 % 10 = 4
So 2025-33-4 is a valid CAS Registry Number.
2025-33-4Relevant articles and documents
The cleavage of 1-amino-2'-nitrobenzylphosphonates in a basic medium. Formation of the 3-amino-2,1-benzisoxazole derivatives
Boduszek, Bogdan,Halama, Agnieszka,Zon, Jerzy
, p. 11399 - 11410 (2007/10/03)
Treatment of 1-amino-2'-nitrobenzylphosphonic acids with aqueous sodium hydroxide caused a C-P bond cleavage, with formation of 3-amino-2,1-benzisoxazole derivatives (3). The leaving phosphorus moiety was identified here as phosphoric acid. In the case of basic hydrolysis of corresponding esters, new cyclic phosphorus compounds (derivatives of benzoxazaphosphorin-3,1,2 P(v)-one-2) were obtained. The cyclic products were formed as a result of the subsequent reaction of anthranil derivatives with leaving phosphorus fragment, presumably metaphosphate, These benzoxazaphosphorins (cormpounds 4) were converted by means of aqueous hydrochloric acid to 3-amino-2,1-benzisoxazole derivatives.
