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215597-45-8

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215597-45-8 Usage

General Description

2-(Aminomethyl)cyclopropanecarboxylic acid is a chemical compound with the molecular formula C5H9NO2. It is a derivative of cyclopropane carboxylic acid with an aminomethyl group attached to the cyclopropane ring. 2-(AMINOMETHYL)CYCLOPROPANECARBOXYLIC ACID has potential applications in the pharmaceutical industry, particularly in the development of new drugs and medications. It may also be used as a building block in organic synthesis for the preparation of various pharmaceutical compounds. The compound's unique structure and properties make it a valuable component in the synthesis of biologically active molecules, and it is an important intermediate for the production of pharmaceuticals and other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 215597-45-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,5,9 and 7 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 215597-45:
(8*2)+(7*1)+(6*5)+(5*5)+(4*9)+(3*7)+(2*4)+(1*5)=148
148 % 10 = 8
So 215597-45-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO2/c6-2-3-1-4(3)5(7)8/h3-4H,1-2,6H2,(H,7,8)

215597-45-8Downstream Products

215597-45-8Relevant articles and documents

A novel stereoselective tin-free radical protocol for the enantioselective synthesis of pyrrolidinones and its application to the synthesis of?biologically active GABA-derivatives

Rodríguez-Soria, Verónica,Quintero, Leticia,Sartillo-Piscil, Fernando

, p. 2750 - 2754 (2008/09/19)

Optically pure 4-alkyl-pyrrolin-2-ones were synthesized from chiral N-allyl-α-bromoacetamides in high selective and stereo-controlled fashion, via a sequential 5-exo-trig radical cyclization-hydrogen or bromine atom-transfer process, under non-tin conditi

Resolution and conformational analysis of diastereoisomeric esters of cis- and trans-2-(aminomethyl)-1-carboxycyclopropanes

Duke, Rujee K.,Allan, Robin D.,Chebib, Mary,Greenwood, Jeremy R.,Johnston, Graham A. R.

, p. 2533 - 2548 (2007/10/03)

(1R,2S)-, (1S,2R)-, (1R,2R)- and (1S,2S)-2-(Aminomethyl)-1- carboxycyclopropanes, conformationally restricted analogues of the neurotransmitter γ-aminobutyric acid (GABA), have been resolved by chromatographic separation of the corresponding diastereoisomeric esters which were formed between the cis- and trans-2-(acetamidomethyl)1- carboxycyclopropanes with (R)-(-)-pantolactone. 1H NMR, semi-empirical conformational analysis, ab initio (DFT) structure and NMR shielding tensor calculations of the cis-diastereoisomers allowed the absolute configuration assignments of the cis-amino acids.

Synthesis of &γ-Aminobutyric Acid Analogue of Restricted Conformation. Part 1. The 2-(Aminomethyl)cycloalkaneacetic Acids

Kennewell, Peter D.,Matharu, Saroop S.,Taylor, John B.,Westwood, Robert,Sammes, Peter G.

, p. 2563 - 2570 (2007/10/02)

The synthesis of analogues with restricted rotatin about the C(2)-C(3) bond of γ-aminobutyric acid, namely cis- and trans-2-(aminomethyl)-cyclopropane and -cyclobutanecarboxylic acids and trans-2-(aminomethyl)cyclohexanecarboxylic acid are described.

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