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(+/-)-trans-2-(N-Benzylamino)cyclopentanol is a chiral chemical compound characterized by a cyclopentanol skeleton with a benzylamino group attached to one of the carbon atoms. As a chiral compound, it exists as a pair of enantiomers, which are mirror images of each other. This unique structure makes it a valuable building block in the synthesis of pharmaceuticals and agrochemicals, as it can be used to create complex molecular structures with potential biological activity.

95628-93-6

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95628-93-6 Usage

Uses

Used in Pharmaceutical Industry:
(+/-)-trans-2-(N-Benzylamino)cyclopentanol is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its cyclopentanol skeleton and benzylamino group provide a versatile platform for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, (+/-)-trans-2-(N-Benzylamino)cyclopentanol serves as a starting material for the creation of biologically active compounds with pesticidal properties. Its ability to participate in a variety of chemical reactions allows for the formation of a wide range of derivatives with potential use in crop protection and management.
Used in Organic Synthesis:
(+/-)-trans-2-(N-Benzylamino)cyclopentanol is utilized as a valuable tool in organic synthesis, particularly for the preparation of complex molecular structures. Its versatility in participating in various chemical reactions makes it an ideal candidate for the development of novel compounds with potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 95628-93-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,6,2 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 95628-93:
(7*9)+(6*5)+(5*6)+(4*2)+(3*8)+(2*9)+(1*3)=176
176 % 10 = 6
So 95628-93-6 is a valid CAS Registry Number.

95628-93-6Relevant academic research and scientific papers

Synthesis of a rigidified bicyclic AAZTA-like ligand and relaxometric characterization of its GdIII complex

Martinelli, Jonathan,Martorana, Enrico,Tei, Lorenzo

, (2020)

The synthesis of a novel constrained polydentate ligand CpAAZTA derived from the heptadentate polyaminocarboxylic ligand AAZTA (6-amino-6-methylperhydro-1,4-diazepine-N, N’,N’’,N’’-tetraacetic acid) in which the ethylene bridge of the 1,4-diazepine ring i

Substituted Imidazopyridines as HDM2 Inhibitors

-

Paragraph 0816, (2014/07/08)

The present invention provides substituted imidazopyridines as described herein or a pharmaceutically acceptable salt or solvate thereof. The representative compounds are useful as inhibitors of the HDM2 protein. Also disclosed are pharmaceutical compositions comprising the above compounds and potential methods of treating cancer using the same.

Syntheses and X-Ray Crystal Structures of Tricyclic Ketones Containing Trans-Fused Azabicyclooctane Units

Mori, Miwako,Saitoh, Fumihiko,Uesaka, Noriaki,Okamura, Kimio,Date, Tadamasa

, p. 4993 - 4998 (2007/10/02)

Tricyclic ketones containing the trans-fused 3-azabicyclooctane framework were prepared from the reactions of dienes and Cp2ZrBu2, followed by treatment with carbon monoxide.The structures were confirmed by X-ray analysis.

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