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(6S)-bicyclo[2.2.1]hept-2-ene-6-carbonitrile, also known as norcarane nitrile, is a bicyclic organic compound characterized by its carbonitrile functional group. It is renowned for its high stability, allowing for long-term storage without degradation or loss of potency. The unique structure and properties of (6S)-bicyclo[2.2.1]hept-2-ene-6-carbonitrile render it an indispensable building block in the synthesis of complex molecules, particularly in the pharmaceutical and agrochemical industries. Moreover, its potential extends to the development of new materials and the realm of organic electronics.

2890-96-2

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2890-96-2 Usage

Uses

Used in Pharmaceutical Industry:
(6S)-bicyclo[2.2.1]hept-2-ene-6-carbonitrile is utilized as an intermediate in organic synthesis for the production of various pharmaceuticals. Its unique bicyclic structure and carbonitrile group contribute to the development of novel drug molecules with enhanced therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, (6S)-bicyclo[2.2.1]hept-2-ene-6-carbonitrile serves as a key intermediate in the synthesis of agrochemicals. Its incorporation into these compounds can lead to the creation of more effective and targeted pest control agents.
Used in Material Development:
(6S)-bicyclo[2.2.1]hept-2-ene-6-carbonitrile is employed in the development of new materials due to its stable and versatile chemical properties. Its integration into material compositions can result in the creation of innovative materials with unique characteristics and applications.
Used in Organic Electronics:
(6S)-bicyclo[2.2.1]hept-2-ene-6-carbonitrile also finds application in the field of organic electronics, where its stable and conductive properties can be harnessed to develop new electronic devices and components with improved performance and efficiency.

Check Digit Verification of cas no

The CAS Registry Mumber 2890-96-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,9 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2890-96:
(6*2)+(5*8)+(4*9)+(3*0)+(2*9)+(1*6)=112
112 % 10 = 2
So 2890-96-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N/c9-5-8-4-6-1-2-7(8)3-6/h1-2,6-8H,3-4H2/t6?,7?,8-/m1/s1

2890-96-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name bicyclo[2.2.1]hept-2-ene-5-carbonitrile

1.2 Other means of identification

Product number -
Other names bicyclo[2.2.1]hept-5-en-2-exo-carbonitrile

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:2890-96-2 SDS

2890-96-2Relevant academic research and scientific papers

Enhanced Diels-Alder reactions: on the role of mineral catalysts and microwave irradiation in ionic liquids as recyclable media

López, Ignacio,Silvero, Guadalupe,Arévalo, María José,Babiano, Reyes,Palacios, Juan?Carlos,Bravo, José Luis

, p. 2901 - 2906 (2007/10/03)

This manuscript explores in detail the combined effect of solid supports or microwave irradiation in ionic liquids on a series of Diels-Alder reactions involving 1,3-cyclopentadiene and numerous dienophiles.

Experimental evidence to support viscosity dependence of rates of Diels-Alder reactions in solvent media

Kumar, Anil,Deshpande, Suvarna S.

, p. 5411 - 5414 (2007/10/03)

This note is aimed at ascertaining whether rates of Diels-Alder reactions depend on the viscosity of solvent media in which the reactions are performed. On the basis of the data collected from the literature and in this laboratory, it is seen in general that the rates increase in the solvents with their viscosities ranging up to ~1.2 cP. In solvents possessing viscosities above 1.2 cP, a drop in the reaction rates is observed in all cases. The effect of temperature on the above phenomena is also examined.

Rearrangements of 5- and 6-Cyano-2-norbornyl Cations

Fermann, Michael,Herpers, Ekkehard,Kirmse, Wolfgang,Neubauer, Regina,Renneke, Franz-Josef,et al.

, p. 975 - 984 (2007/10/02)

Hydroboration of the 5-norbornene-2-carbonitriles 11 afforded 5- and 6-hydroxynorbornane-2-carbonitriles (9a, 10a) along with the analogous ketones 12, 13. 5- and 6-aminonorbornane-2-carbonitriles (17a, 18a) were obtained either from the endo-brosylates 1

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