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225641-82-7

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225641-82-7 Usage

General 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 commonly used in the pharmaceutical industry as a prodrug for the production of various medications. Carbamic acid, [(1S,3R)-3-(acetyloxy)cyclopentyl]-, 1,1-dimethylethyl ester is a bidentate ligand that forms stable chelates with various metal ions, making it useful in coordination chemistry. It has also shown potential as an antitumor agent and is being researched for its potential use in cancer therapy. Additionally, it has been investigated for its potential as a biodegradable insecticide due to its relatively low toxicity to mammals. Overall, Carbamic acid, [(1S,3R)-3-(acetyloxy)cyclopentyl]-, 1,1-dimethylethyl ester has a wide range of potential applications in various fields due to its versatile chemical properties.

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.

225641-82-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,3S)-3-((tert-butoxycarbonyl)amino)cyclopentyl acetate

1.2 Other means of identification

Product number -
Other names -

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:225641-82-7 SDS

225641-82-7Relevant articles and documents

Method for preparing (1R, 3S)-3-aminocyclopentanol hydrochloride

-

, (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.

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