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1,6-Diaminodiamantane is a polycyclic diamine synthesized from 1,6-dibromodiamantane via a two-step process involving acetonitrile and sulfuric acid to form 1,6-diacetamidodiamantane, followed by hydrolysis with NaOH to yield the final product. 1,6-diaminodiamantane represents a structurally rigid diamine with potential applications in materials science or medicinal chemistry due to its diamondoid framework.

166040-10-4

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166040-10-4 Usage

Type of compound

Diamantane derivative

Structure

Diamond-like structure

Physical state at room temperature

White solid

Properties

a. High thermal stability
b. Chemical resistance

Potential applications

a. Materials science
b. Building block for novel organic compounds
c. Pharmaceutical intermediate (due to unique structure and potential biological activity)

Interest

Generated due to its interesting molecular structure and potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 166040-10-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,0,4 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 166040-10:
(8*1)+(7*6)+(6*6)+(5*0)+(4*4)+(3*0)+(2*1)+(1*0)=104
104 % 10 = 4
So 166040-10-4 is a valid CAS Registry Number.

166040-10-4Downstream Products

166040-10-4Relevant academic research and scientific papers

Synthetic routes to aminotriamantanes, topological analogues of the neuroprotector Memantine

Fokin, Andrey A.,Merz, Anika,Fokina, Natalie A.,Schwertfeger, Hartmut,Liu, Shenggao L.,Dahl, Jeremy E. P.,Carlson, Robert K. M.,Schreiner, Peter R.

, p. 909 - 912 (2009)

The amino derivatives of diamantane and triamantane, representing close topological analogues of the neuroprotective drug Memantine, were prepared via amination of the respective carboxylic acids or alcohols. Georg Thieme Verlag Stuttgart.

Synthesis of 1,6-diaminodiamantane

Chern,Wang

, p. 5805 - 5806 (1995)

A new polycyclic diamine, 1,6-diaminodiamantane, was synthesized starting from 1,6-dibromodiamantane. The reaction of 1,6-dibromodiamantane with acetonitrile using H2SO4 as catalyst afforded 1,6-diacetamidodiamantane in 72% yield. The reaction of 1,6-diacetamidodiamantane with NaOH afforded 1,6-diaminodiamantane in 50% yield.

Preparation of diamines of adamantane and diamantane from the diazides

Davis, Matthew,Nissan, David

, p. 2113 - 2119 (2007/10/03)

A novel synthetic method for preparing diaminodiamondoids from diazidodiamondoids starting from the hydrocarbons is described. Copyright Taylor & Francis Group, LLC.

Diamondoid derivatives possessing therapeutic activity in the treatment of neurologic disorders

-

Page/Page column 25, (2008/06/13)

This invention relates to diamondoid derivatives which exhibit therapeutic activity. Specifically, the diamondoid derivatives herein exhibit therapeutic effects in the treatment of neurologic disorders. Also provided are methods of treatment, prevention a

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