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39234-37-2

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39234-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39234-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,2,3 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 39234-37:
(7*3)+(6*9)+(5*2)+(4*3)+(3*4)+(2*3)+(1*7)=122
122 % 10 = 2
So 39234-37-2 is a valid CAS Registry Number.
InChI:InChI=1/C17H23N/c1-2-4-12(5-3-1)11-18-17-15-7-13-6-14(9-15)10-16(17)8-13/h1-5,13-18H,6-11H2

39234-37-2SDS

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 2-(N-Benzylamino)adamantane

1.2 Other means of identification

Product number -
Other names -

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:39234-37-2 SDS

39234-37-2Relevant academic research and scientific papers

MULTICYCLIC COMPOUNDS AND USE OF SAME FOR TREATING TUBERCULOSIS

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Paragraph 00205; 00206, (2019/07/30)

Provided herein are multicyclic compounds useful for treating tuberculosis. Also provided are methods of treating tuberculosis using the compounds of the invention.

COMPOUNDS WHICH HAVE A PROTECTIVE ACTIVITY WITH RESPECT TO THE ACTION OF TOXINS AND OF VIRUSES WITH AN INTRACELLULAR MODE OF ACTION

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Paragraph 0175; 0176, (2016/04/19)

The subject matter of the present invention is novel families of compounds which are aromatic amine, imine, aminoadamantane and benzodiazepine derivatives, medicaments comprising same and the use thereof as inhibitors of the toxic effects of toxins with intracellular activity, such as, for example, ricin, and of viruses that use the internalization pathway for infecting cells.

Copper-nitrene complexes in catalytic C-H amination

Badiei, Yosra M.,Dinescu, Adriana,Dai, Xuliang,Palomino, Robert M.,Heinemann, Frank W.,Cundari, Thomas R.,Warren, Timothy H.

supporting information; experimental part, p. 9961 - 9964 (2009/05/07)

(Chemical Equation Presented) Hydrocarbons activate! Isolable β-diketiminato dicopper-nitrene complexes such as 1 derived from the reaction of [{(Cl2NN)Cu}2(μ-benzene)] and 1-adamantylazide are potent towards nitrene insertion into unactivated sp 3-hybridized C-H bonds. 1 allows stoichiometric and catalytic intermolecular C-H amination of hydrocarbons to give secondary amines (see scheme). Catalyst loadings as low as 0.05 mol% may be used.

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