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225641-86-1

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225641-86-1 Usage

Description

Carbamic acid, [(1R)-3-oxocyclopentyl]-, 1,1-dimethylethyl ester (9CI), also known as tert-butyl (1R)-3-oxocyclopentylcarbamate, is a chemical compound that belongs to the carbamic acid ester class. It is a colorless liquid with a molecular formula of C10H17NO3 and a molecular weight of 199.25 g/mol. Carbamic acid, [(1R)-3-oxocyclopentyl]-, 1,1-dimethylethyl ester (9CI) is commonly used as a reagent in organic synthesis and serves as a building block in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.

Uses

Used in Pharmaceutical Industry:
Carbamic acid, [(1R)-3-oxocyclopentyl]-, 1,1-dimethylethyl ester (9CI) is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, Carbamic acid, [(1R)-3-oxocyclopentyl]-, 1,1-dimethylethyl ester (9CI) is utilized as a key intermediate in the synthesis of agrochemicals, such as pesticides and herbicides. Its incorporation into these products helps enhance their effectiveness in controlling pests and weeds, thereby improving crop yields and quality.
Used in Specialty Chemicals Production:
Carbamic acid, [(1R)-3-oxocyclopentyl]-, 1,1-dimethylethyl ester (9CI) is also employed in the production of specialty chemicals, which are high-value chemicals used in various applications, such as coatings, adhesives, and polymers. Its unique properties contribute to the development of innovative and high-performance specialty chemicals that meet specific industry requirements.
Used as a Reagent in Organic Synthesis:
In addition to its applications in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals, Carbamic acid, [(1R)-3-oxocyclopentyl]-, 1,1-dimethylethyl ester (9CI) is also used as a reagent in organic synthesis. Its reactivity and versatility make it a valuable tool for chemists in the development of new organic compounds and the optimization of existing synthetic routes.

Check Digit Verification of cas no

The CAS Registry Mumber 225641-86-1 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 225641-86:
(8*2)+(7*2)+(6*5)+(5*6)+(4*4)+(3*1)+(2*8)+(1*6)=131
131 % 10 = 1
So 225641-86-1 is a valid CAS Registry Number.

225641-86-1SDS

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 tert-butyl N-[(1R)-3-oxocyclopentyl]carbamate

1.2 Other means of identification

Product number -
Other names CARBAMIC ACID,[(1R)-3-OXOCYCLOPENTYL]-,1,1-DIMETHYLETHYL ESTER

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:225641-86-1 SDS

225641-86-1Relevant articles and documents

PYRAZOLO-PYRIMIDIN-AMINO-CYCLOALKYL COMPOUNDS AND THEIR THERAPEUTIC USES

-

Paragraph 0544, (2019/12/28)

Disclosed herein are pyrazolo-pyrimid in-ami no-cycloalkyl compounds, analogs thereof, pharmaceutical compositions comprising thereof and therapeutic uses therefor.

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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