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Cyclopropanecarboxylic acid, 2-methyl-, (1S,2S)is a chiral chemical compound with the molecular formula C6H10O2. It is characterized by its unique cyclopropane ring structure and a methyl group at the 2nd position. The (1S,2S)configuration denotes the specific stereochemistry of the molecule, which is crucial for its properties and applications.

14590-52-4

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14590-52-4 Usage

Uses

Used in Pharmaceutical Industry:
Cyclopropanecarboxylic acid, 2-methyl-, (1S,2S)is used as a building block for the synthesis of various drugs. Its unique structure and chirality make it a valuable component in the development of new pharmaceutical compounds with specific therapeutic effects.
Used in Organic Synthesis:
Cyclopropanecarboxylic acid, 2-methyl-, (1S,2S)is also utilized in the synthesis of other organic compounds, contributing to the diversity of chemical products and materials. Its reactivity and structural features enable the formation of new molecules with potential applications in various fields.
Used as a Reagent in Chemical Reactions:
Cyclopropanecarboxylic acid, 2-methyl-, (1S,2S)serves as a reagent in various chemical reactions, facilitating the formation of desired products and improving the efficiency of synthetic processes. Its presence can influence the outcome of reactions, making it a valuable tool in the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 14590-52-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,9 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14590-52:
(7*1)+(6*4)+(5*5)+(4*9)+(3*0)+(2*5)+(1*2)=104
104 % 10 = 4
So 14590-52-4 is a valid CAS Registry Number.

14590-52-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (1SR,2SR)-2-methylcyclopropanecarboxylic acid

1.2 Other means of identification

Product number -
Other names trans-2-Methyl-1-cyclopropanecarboxylic acid

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:14590-52-4 SDS

14590-52-4Relevant articles and documents

N3-CYCLICALLY SUBSTITUTED THIENOURACILS AND USE THEREOF

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, (2020/02/05)

The present application relates to novel thieno[2,3-d]pyrimidine-2,4-dione (“thienouracil”) derivatives having cyclic substituents in the 3 position, to processes for the preparation thereof, to the use thereof alone or in combinations for treatment and/or prevention of diseases and to the use thereof for production of medicaments for treatment and/or prevention of diseases, especially for treatment and/or prevention of pulmonary and cardiovascular disorders and of cancer.

SUBSTITUTED CARBOXAMIDES

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Page/Page column 16-17, (2008/12/08)

This application relates to a substituted carboxamide compound of formula I, or a pharmaceutically acceptable salt thereof, as defined herein, a pharmaceutical composition thereof, and its use in treating pain.

184. Stereoselective Hydrolysis of Substituted Cyclopropanedicarboxylates with Pig Liver Esterase

Walser, Paula,Renold, Peter,N'Goka, Victor,Hosseinzadeh, Fatemeh,Tamm, Christoph

, p. 1941 - 1952 (2007/10/02)

The hydrolysis of the meso-cyclopropane-1,2-dicarboxylates 1a-3a, 4, 5a, 6a, and 9, containing various substituents at C(3), and of the rac-3-phenylcyclopropane-1,2-dicarboxylates 7a, 8a, and 10 with pig liver esterase (PLE) is described.The stereoselectivity and absolute configurations of the products were determined.An interpretation of results was attempted on the basis of a recent active-site model for PLE.

1-Aryl-2,2-dimethyl-1,3-propanediols as chiral auxiliares. Acetal formation with α,β-unsaturated aldehydes and analysis of the stereochemistry of cyclopropanation

Ebens, Rijko,Kellogg, Richard M.

, p. 552 - 560 (2007/10/02)

Optically pure 1-aryl- (phenyl and 2-chlorophenyl) 1,3-propanediols, 1a and 1b, condense smoothly with aldehydes to provide the corresponding cyclic acetals 3.Except in cases that the aldehyde is substituted at the α-carbon atom, a single product is obtai

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