Welcome to LookChem.com Sign In|Join Free

CAS

  • or
5-NORBONENE-2-METHANAMINE is a chemical compound that belongs to the class of amines. It is a colorless liquid with a strong, pungent odor. 5-NORBONENE-2-METHANAMINE is recognized for its role as an intermediate in the production of various pharmaceuticals and organic compounds, and it serves as a building block in the synthesis of a range of chemical products. Classified as a hazardous substance, 5-NORBONENE-2-METHANAMINE requires careful handling due to its potential toxicity and flammability, necessitating adherence to proper safety protocols to minimize risks.

95-10-3

Post Buying Request

95-10-3 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

95-10-3 Usage

Uses

Used in Pharmaceutical Industry:
5-NORBONENE-2-METHANAMINE is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its role in this industry is crucial for the development of new drugs and the improvement of existing ones, contributing to advancements in medical treatments.
Used in Organic Compounds Production:
In the realm of organic chemistry, 5-NORBONENE-2-METHANAMINE is utilized as a key component in the production of a variety of organic compounds. Its versatility in chemical reactions allows for the creation of diverse products used across different sectors.
Used in Chemical Synthesis:
5-NORBONENE-2-METHANAMINE is employed as a building block in the synthesis of a wide array of chemical products. Its structural properties make it a valuable asset in the development of new chemical entities with potential applications in various industries.
Safety Considerations:
Given its classification as a hazardous substance, 5-NORBONENE-2-METHANAMINE is used with strict adherence to safety protocols. This includes measures to prevent exposure, control flammability, and manage potential toxic effects, ensuring the safety of workers and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 95-10-3 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 5 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 95-10:
(4*9)+(3*5)+(2*1)+(1*0)=53
53 % 10 = 3
So 95-10-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H13N/c9-5-8-4-6-1-2-7(8)3-6/h1-2,6-8H,3-5,9H2

95-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Bicyclo[2.2.1]hept-5-en-2-ylmethanamine

1.2 Other means of identification

Product number -
Other names 5-bicyclo[2.2.1]hept-2-enylmethanamine

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:95-10-3 SDS

95-10-3Relevant articles and documents

Supporting multiple organometallic catalysts on poly(norbornene) for cyanide addition to α,β-unsaturated imides

Madhavan, Nandita,Sommer, William,Weck, Marcus

experimental part, p. 1 - 7 (2011/03/16)

A two-catalyst system comprising of salen(AlCl) and pybox(ErCl3) complexes supported onto poly(norbornene) has been developed. As a proof of concept the activity of the two-catalyst system was gauged for the addition of cyanide to α,β-unsaturated imides which has been shown to follow a bimetallic mechanism. The activity of the supported two-catalyst system was significantly higher than catalytic systems derived from mixtures of the two catalysts. In addition, the co-polymer could be readily recovered and reused up to 3 cycles without significant loss in conversions and yields. Nevertheless, a decrease in enantioselectivity of the cyanide adduct was observed with each subsequent cycle indicating some loss in catalytic selectivity. The reported strategy opens up avenues for supporting multiple catalysts on the same polymer backbone for catalyst-based one-pot cascade reactions.

Process for forming perfluorinated-alkyl sulfonamide substituted norbornene-type monomers

-

Page/Page column 1-3, (2008/06/13)

Embodiments in accordance with the present invention are directed to providing processes for forming fluorinated-alkyl and particularly perfluorinated-alkyl sulfonamide substituted norbornene-type monomers.

Fluorinated Sulfonamides of the Norbornene Series

Kas'yan, A. O.,Maletina, I. I.,Yagupol'skii, L. M.,Markov, V. I.,Kas'yan, L. I.

, p. 320 - 327 (2007/10/03)

Fluorinated sulfonamides derived from exo- and endo-5-aminomethylbicyclohept-2-ene have been prepared and studied.These compounds were synthesized from pure isomers of bicyclohept-2-ene-5-carbonitrile obtained by Diels-Alder reaction from cyclopentadiene and acrylonitrile.The influence of the substituent orientation in the norbornene moiety on the 1H NMR spectra of stereoisomeric sulfonamides has been studied.Reactions of both isomers of N-(perfluorobutylsulfonyl)-5-aminomethylbicyclohept-2-ene with peroxy acids yield epoxides as the only reaction products.The intramolecular cyclization product is not formed, probably owing to the low nucleophilicity (basicity) of the nitrogen atom bearing the perfluorosulfonyl group.

Urea and Thiourea Derivatives Based on Amines of the Norbornene Series

Kas'yan, A. O.,Krasnovskaya, O. Yu.,Okovityi, S. I.,Kas'yan, L. I.

, p. 311 - 319 (2007/10/03)

Electron density distribution in molecules of amino derivatives of norbornene, exo- and endo-5-aminomethylbicyclohept-2-ene, exo-5-aminomethyl-endo-5-methylbicyclohept-2-ene, and their epoxy derivatives was studied by spectral methods (IR and 1H, 13C, and two-dimensional NMR spectroscopy) and by semiempirical (AM1) quantum-chemical calculations.The reactivity of amines was preliminary estimated from the calculated parameters: proton affinity and energies of localized molecular orbitals.The nucleophilic properties of the amines were studied in reactions with acyclic, alicyclic, and aromatic isocyanates and isothiocyanates.In the series of potentially bioactive ureas and thioureas, criteria have been formulated for ascribing the exo and endo structures to these compounds on the basis of the 1H NMR spectra.

Asymmetric Diels-Alder Reaction Using (S)-Pyroglutamic Acid Derivatives as Chiral Dienophiles

Ikota, Nobuo

, p. 2219 - 2221 (2007/10/02)

Asymmetric Diels-Alder reaction of cyclopentadiene with chiral dienophiles (3) derived from (S)-pyroglutamic acid derivatives was performed in the presence of a Lewis acid such as diethylaluminium chloride in toluene to afford the cycloadducts with high diastereoselectivity.Keywords asymmetric reaction; Diels-Alder reaction; (S)-pyroglutamic acid; chiral dienophile; diethylaluminium chloride; (2+4)cycloaddition

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 95-10-3