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(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, featuring a pyrrolidin-3-yl-ethyl substituent. (2-Pyrrolidin-3-yl-ethyl)-carbamic acid benzyl ester is recognized for its potential applications in the pharmaceutical and agrochemical industries, as well as in organic synthesis and as a reagent in chemical reactions.

2025-33-4

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2025-33-4 Usage

Uses

Used in Pharmaceutical Industry:
(2-Pyrrolidin-3-yl-ethyl)-carbamic acid benzyl ester serves as an intermediate in the synthesis of various pharmaceutical drugs. Its role in drug development is crucial, as it contributes to the formation of active pharmaceutical ingredients (APIs) that address a range of health conditions.
Used in Agrochemical Industry:
In the agrochemical sector, (2-Pyrrolidin-3-yl-ethyl)-carbamic acid benzyl ester is utilized as an intermediate in the production of agrochemicals. These chemicals are essential for developing pesticides, herbicides, and other products that protect crops and enhance agricultural productivity.
Used in Organic Synthesis:
(2-Pyrrolidin-3-yl-ethyl)-carbamic acid benzyl ester is also employed in organic synthesis, where it acts as a building block for creating more complex organic molecules. Its unique structure allows it to participate in various chemical reactions, facilitating the synthesis of a wide array of organic compounds.
Used as a Reagent in Chemical Reactions:
Furthermore, (2-Pyrrolidin-3-yl-ethyl)-carbamic acid benzyl ester functions as a reagent in numerous chemical reactions. Its participation in these processes is vital for achieving desired outcomes and producing specific chemical products.
Used in Neurodegenerative Disorder Treatment:
(2-Pyrrolidin-3-yl-ethyl)-carbamic acid benzyl ester has been studied for its potential as a cholinesterase inhibitor. This characteristic makes it a compound of interest for the treatment of Alzheimer's disease and other neurodegenerative disorders, where it may help improve cognitive function by increasing the levels of the neurotransmitter acetylcholine in the brain.
Precaution:
It is important to handle and use (2-Pyrrolidin-3-yl-ethyl)-carbamic acid benzyl ester with care, as it may pose health and environmental hazards. Proper safety measures should be taken to minimize any risks associated with its use.

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.

2025-33-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,1-benzoxazol-3-amine

1.2 Other means of identification

Product number -
Other names 3-Amino-benzisoxazol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2025-33-4 SDS

2025-33-4Upstream product

2025-33-4Relevant academic research and scientific papers

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.

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