225641-82-7 Usage
Description
Carbamic acid, [(1S,3R)-3-(acetyloxy)cyclopentyl]-, 1,1-dimethylethyl ester is a chemical compound with the chemical formula C12H21NO4. It is a derivative of carbamic acid and is known for its versatile chemical properties. Carbamic acid, [(1S,3R)-3-(acetyloxy)cyclopentyl]-, 1,1-dimethylethyl ester serves as a bidentate ligand, capable of forming stable chelates with various metal ions, which is particularly useful in coordination chemistry. Additionally, it has demonstrated potential as both an antitumor agent and a biodegradable insecticide due to its relatively low toxicity to mammals.
Uses
Used in Pharmaceutical Industry:
Carbamic acid, [(1S,3R)-3-(acetyloxy)cyclopentyl]-, 1,1-dimethylethyl ester is utilized as a prodrug in the pharmaceutical industry for the production of various medications. Its ability to form stable chelates with metal ions makes it a valuable component in the development of drugs with enhanced efficacy and targeted action.
Used in Coordination Chemistry:
In coordination chemistry, this compound functions as a bidentate ligand, forming stable chelates with different metal ions. This property is exploited in the design and synthesis of coordination compounds for various applications, including catalysts, sensors, and materials with unique properties.
Used in Cancer Therapy Research:
Carbamic acid, [(1S,3R)-3-(acetyloxy)cyclopentyl]-, 1,1-dimethylethyl ester has shown potential as an antitumor agent. It is currently being researched for its possible use in cancer therapy, where its ability to interact with metal ions could play a role in the development of novel treatment strategies.
Used in Agricultural Applications:
Due to its potential as a biodegradable insecticide, this compound is being investigated for use in agriculture. Its relatively low toxicity to mammals makes it a promising candidate for the development of safer and more environmentally friendly pest control solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 225641-82-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,6,4 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 225641-82:
(8*2)+(7*2)+(6*5)+(5*6)+(4*4)+(3*1)+(2*8)+(1*2)=127
127 % 10 = 7
So 225641-82-7 is a valid CAS Registry Number.
225641-82-7Relevant articles and documents
Method for preparing (1R, 3S)-3-aminocyclopentanol hydrochloride
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, (2021/03/31)
The invention discloses a method for preparing (1R, 3S) 3-aminocyclopentanol hydrochloride, belongs to the field of organic chemical synthesis, and provides a process route to overcome the defects ofhigh price, difficulty in chiral control and the like in the prior art. The process route comprises the following steps: 1) oxidizing tert-butyl carbonate hydroxylamine into tert-butyl carbonate nitrosyl under the catalysis of copper chloride and 2-ethyl-2-oxazoline, then carrying out a hetero Diels-Alder reaction with cyclopentadiene in situ; 2) selectively reducing nitrogen-oxygen bonds in a zinc powder-acetic acid reaction system; 3) under the catalysis of lipase, reacting with vinyl acetate to optically and selectively realize chiral resolution; 4) reducing double bonds through palladium carbon hydrogenation; 5) under the alkaline condition of lithium hydroxide-methanol, performing deacetylation protection; and 6) removing tert-butyl carbonate protection in a hydrogen chloride isopropanol acid solution prepared from acetyl chloride and isopropanol in situ, and forming hydrochloride in situ to obtain a target product. The synthetic method has the beneficial effects that the synthetic method has the characteristics of novel and short route, high optical purity, low cost and the like.
Preparation and evaluation of 1,3-diaminocyclopentane-linked dihydropyrimidinone derivatives as selective α(1a)-receptor
Barrow, James C.,Glass, Kristen L.,Selnick, Harold G.,Freidinger, Roger M.,Chang, Raymond S.L.,O'Malley, Stacey S.,Woyden, Carla
, p. 1917 - 1920 (2007/10/03)
Several 1,3-diaminocyclopentane linked α(1a)-receptor antagonists were prepared using a divergent chemical strategy that allows for rapid analysis of all stereochemical permutations for their effect on α1-receptor binding. (C) 2000 Published by Elsevier Science Ltd.
