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1822-25-9

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1822-25-9 Usage

General Description

1-Bromo-3-(bromomethyl)adamantane is a chemical compound with the molecular formula C10H15Br2. It is a brominated derivative of adamantane, which is a highly stable and rigid hydrocarbon molecule. The presence of two bromine atoms in this compound makes it a potential reagent for various chemical reactions, particularly in the synthesis of organic compounds. The bromine atoms in this compound can act as electrophiles, participating in substitution and addition reactions. 1-Bromo-3-(bromomethyl)adamantane has been used in research and industrial applications, but it also presents potential hazards due to its bromine content, requiring proper handling and disposal procedures.

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

1822-25-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-BROMO-3-(BROMOMETHYL)ADAMANTANE

1.2 Other means of identification

Product number -
Other names 3-Brom-1-brommethyl-adamantan

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:1822-25-9 SDS

1822-25-9Downstream Products

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.

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