1822-25-9 Usage
Description
1-Bromo-3-(bromomethyl)adamantane, with the molecular formula C10H15Br2, is a brominated derivative of the highly stable and rigid hydrocarbon molecule, adamantane. Characterized by the presence of two bromine atoms, this compound serves as a versatile reagent in various chemical reactions, particularly in the synthesis of organic compounds. The bromine atoms in 1-Bromo-3-(bromomethyl)adamantane can function as electrophiles, engaging in substitution and addition reactions, making it valuable for research and industrial applications. However, its bromine content also poses potential hazards, necessitating careful handling and disposal.
Uses
Used in Chemical Synthesis:
1-Bromo-3-(bromomethyl)adamantane is used as a reagent in chemical synthesis for its ability to participate in substitution and addition reactions due to the electrophilic nature of its bromine atoms. This makes it suitable for the creation of a variety of organic compounds.
Used in Research Applications:
In the field of research, 1-Bromo-3-(bromomethyl)adamantane is utilized as a model compound to study the properties and reactions of brominated hydrocarbons, contributing to the understanding of chemical behavior and the development of new synthetic pathways.
Used in Industrial Applications:
1-Bromo-3-(bromomethyl)adamantane is employed in industrial processes where its unique structural and chemical properties are leveraged for the production of specific organic compounds or materials, such as pharmaceuticals or specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 1822-25-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,2 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1822-25:
(6*1)+(5*8)+(4*2)+(3*2)+(2*2)+(1*5)=69
69 % 10 = 9
So 1822-25-9 is a valid CAS Registry Number.
InChI:InChI=1/C11H16Br2/c12-7-10-2-8-1-9(3-10)5-11(13,4-8)6-10/h8-9H,1-7H2
1822-25-9Relevant articles and documents
Synthese de quelques structures encombrees derivees de l'adamantane et de ses analogues par alkylation des ether d'enol trimethylsilyliques
Dubois, Jacques-Emile,Lebbar, Kadija,Lion, Claude,Dugast, Jean-Yves
, p. 905 - 910 (2007/10/02)
Alkylation of trimethylsilyl enol ethers of 2,4-dimethyl-3-pentanone, cyclopentanone and cyclohexanone has been extended to alkylating agents with a cage structure (substituted or functionalized adamantyl, diamantyl, homoadamantyl and noradamantyl chlorides or bromides).This method affords some new cage structured aliphatic and alicyclic ketones.In some cases one observes a new TiCl4 promoted reaction where the bromine in the alkylating agent is replaced by chlorine.This work is a generalization of our previous extended studies on α-alkylation of ketones with tertiary alkylating agents.
