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CyclopenteniMine is an organic compound that serves as a key intermediate in the synthesis of various pharmaceuticals and chemical compounds. It is known for its unique chemical properties and reactivity, making it a valuable building block in the development of new drugs and materials.

285-63-2

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285-63-2 Usage

Uses

Used in Pharmaceutical Industry:
CyclopenteniMine is used as a key intermediate for the novel synthesis of Tamiflu, an antiviral medication used to treat and prevent influenza A and B. Its unique chemical structure allows for the efficient production of this important drug, contributing to the fight against viral infections.
Used in Chemical Industry:
CyclopenteniMine is also used in the preparation of aziridines, which are versatile building blocks in organic chemistry. Aziridines are valuable for the synthesis of a wide range of compounds, including pharmaceuticals, agrochemicals, and advanced materials. The use of CyclopenteniMine in this context highlights its importance in the development of new and innovative products across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 285-63-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,8 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 285-63:
(5*2)+(4*8)+(3*5)+(2*6)+(1*3)=72
72 % 10 = 2
So 285-63-2 is a valid CAS Registry Number.

285-63-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Azabicyclo[3.1.0]hexane

1.2 Other means of identification

Product number -
Other names Cyclopentenimine

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:285-63-2 SDS

285-63-2Relevant academic research and scientific papers

Titanium and Cobalt Bimetallic Radical Redox Relay for the Isomerization of N -Bz Aziridines to Allylic Amides

Wood, Devin P.,Guan, Weiyang,Lin, Song

supporting information, p. 4213 - 4220 (2021/08/10)

Herein a bimetallic radical redox-relay strategy is employed to generate alkyl radicals under mild conditions with titanium(III) catalysis and terminated via hydrogen atom transfer with cobalt(II) catalysis to enact base-free isomerizations of N-Bz aziridines to N-Bz allylic amides. This reaction provides an alternative strategy for the synthesis of allylic amides from alkenes via a three-step sequence to accomplish a formal transpositional allylic amination.

Copper-catalyzed ring-opening reactions of alkyl aziridines with b2 pin2: Experimental and computational studies

Boldrini, Cosimo,Comparini, Lucrezia Margherita,Di Bussolo, Valeria,Di Pietro, Sebastiano,Favero, Lucilla,Menichetti, Andrea,Pineschi, Mauro

, (2021/12/17)

The possibility to form new C–B bonds with aziridines using diboron derivatives con-tinues to be a particularly challenging field in view of the direct preparation of functionalized β-aminoboronates, which are important compounds in drug discovery, being a bioisostere of β-aminoacids. We now report experimental and computational data that allows the individua-tion of the structural requisites and of reaction conditions necessary to open alkyl aziridines using bis(pinacolate)diboron (B2 pin2 ) in a regioselective nucleophilic addition reaction under copper catalysis.

Activation of carboxylic acids in asymmetric organocatalysis

Monaco, Mattia Riccardo,Poladura, Belen,Diaz De Los Bernardos, Miriam,Leutzsch, Markus,Goddard, Richard,List, Benjamin

, p. 7063 - 7067 (2014/07/08)

Organocatalysis, catalysis using small organic molecules, has recently evolved into a general approach for asymmetric synthesis, complementing both metal catalysis and biocatalysis.1 Its success relies to a large extent upon the introduction of novel and generic activation modes.2 Remarkably though, while carboxylic acids have been used as catalyst directing groups in supramolecular transition-metal catalysis,3 a general and well-defined activation mode for this useful and abundant substance class is still lacking. Herein we propose the heterodimeric association of carboxylic acids with chiral phosphoric acid catalysts as a new activation principle for organocatalysis. This self-assembly increases both the acidity of the phosphoric acid catalyst and the reactivity of the carboxylic acid. To illustrate this principle, we apply our concept in a general and highly enantioselective catalytic aziridine-opening reaction with carboxylic acids as nucleophiles. Activation by dimerization: There is still no general activation mode for carboxylic acids in organocatalysis. The formation of heterodimers between chiral phosphoric acid diesters and carboxylic acids can be used to activate and direct reactivity of the latter in asymmetric reactions. This novel principle has been applied to the ring-opening desymmetrization and kinetic resolution of aziridines leading to valuable amino alcohols.

Scalable synthesis of N -acylaziridines from N -tosylaziridines

Rubin, Heather,Cockrell, Jennifer,Morgan, Jeremy B.

, p. 8865 - 8871 (2013/09/24)

N-Acylaziridines are important starting materials for the synthesis of chiral amine derivatives. The traditional methods for producing these activated aziridines have significant drawbacks. The gram scale synthesis of N-acylaziridines by deprotection of N

Chemoenzymatic synthesis of optically active cis- and trans-2-(1H-Imidazol- 1-yl)cycloalkanamines

Alatorre-Santamaria, Sergio,Gotor-Fernandez, Vicente,Gotor, Vicente

experimental part, p. 1057 - 1063 (2011/04/17)

The preparation of enantiopure 2-(1H-imidazol-1-yl)cycloalkanamines has been studied by independent chemoenzymatic approaches. We first explored a route involving the enzymatic resolution of racemic cycloalkanol analogs for the preparation of the correspo

Ring-opening of NH-aziridines with thiols in ionic liquids: Application to the synthesis of aminosulfide catalysts for asymmetric epoxidation of aldehydes

Namutebi, Mariam,McGarrigle, Eoghan M.,Aggarwal, Varinder K.

scheme or table, p. 1250 - 1272 (2010/08/21)

The ring opening of NH-aziridines with thiols was found to proceed in good yield at room temperature in the presence of an ionic liquid1-butyl-3- methylimidazolium chloride (BMIM chloride). This mild methodology was applied to the synthesis of a camphor-derived chiral aminosulfide. The sulfide was used to generate a sulfur ylide, which effected an asymmetric epoxidation of benzaldehyde (e.r. 85:15, trans:cis 90:10, 87% yield). The amino group enabled easy recovery of the sulfide (98% yield) after the reaction by a simple acid/base extraction. Copyright Taylor & Francis Group.

Enantioselective desymmetrization of meso-aziridines with TMSN3 or TMSCN catalyzed by discrete yttrium complexes

Wu, Bin,Gallucci, Judith C.,Parquette, Jon R.,RajanBabu

supporting information; experimental part, p. 1126 - 1129 (2009/06/20)

(Chemical Equation Presented) Y is it so? Dimeric yttrium-salen complexes (see structure; N blue, O red, Y magenta) catalyze the highly enantioselective ring-opening of meso-aziridines by TMSCN and TMSN3. To explain the dramatic differences in

Enantioselective ring-opening of aziridines

-

Page/Page column 15, (2009/02/11)

A process for the preparation of a nucleophilic addition product of an aziridine and a nucleophile, the process comprising treating the arizidine with the nucleophile in the presence of a biaryl phosphoric acid catalyst

Bronsted acid-catalyzed desymmetrization of meso-aziridines

Rowland, Emily B.,Rowland, Gerald B.,Rivera-Otero, Edwin,Antilla, Jon C.

, p. 12084 - 12085 (2008/04/11)

The enantioselective ring-opening of meso-aziridines with azide nucleophiles proceeded in the presence of a catalytic amount of a chiral phosphoric acid catalyst. The reaction affords the formation of the products in excellent yield and enantioselectivity. Preliminary mechanistic studies indicate that the active catalytic species is a chiral silane that is generated in situ. Copyright

Asymmetric Catalysis by Vitamin B12: The Isomerization of Achiral Aziridines to Optically Active Allylic Amines

Zhang, Zhong da,Scheffold, Rolf

, p. 2602 - 2615 (2007/10/02)

Achiral N-acylaziridines are isomerized to optically active N-acyl-allylamines in ee's of up to 95percent by catalytic amounts of cob(I)alamin in MeOH.

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