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2,12-Dibromocyclododecanone, with the molecular formula C12H20Br2O, is a cyclic ketone featuring a 12-carbon ring structure with two bromine atoms attached. This chemical compound is recognized for its mild and selective oxidizing properties, making it a versatile reagent in organic synthesis.

24459-40-3

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24459-40-3 Usage

Uses

Used in Organic Synthesis:
2,12-Dibromocyclododecanone is utilized as a reagent in organic synthesis, leveraging its unique chemical structure and reactivity to facilitate the production of various other chemicals.
Used in Pharmaceutical and Agrochemical Industries:
As an intermediate, 2,12-Dibromocyclododecanone plays a crucial role in the manufacture of pharmaceuticals and agrochemicals, contributing to the development of new and improved products in these fields.
Used in Research:
In the realm of scientific research, 2,12-Dibromocyclododecanone serves as a building block in the synthesis of complex organic molecules, enabling the exploration of novel chemical pathways and the creation of innovative compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 24459-40-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,5 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24459-40:
(7*2)+(6*4)+(5*4)+(4*5)+(3*9)+(2*4)+(1*0)=113
113 % 10 = 3
So 24459-40-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H20Br2O/c13-10-8-6-4-2-1-3-5-7-9-11(14)12(10)15/h10-11H,1-9H2

24459-40-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,12-dibromocyclododecan-1-one

1.2 Other means of identification

Product number -
Other names Cyclododecanone, 2,12-dibromo-

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:24459-40-3 SDS

24459-40-3Upstream product

24459-40-3Relevant academic research and scientific papers

On Triazoles XXXI. The Reaction of 1,2,4-Triazolylcarbothiohydrazides with Homo- and Heterocyclic Ketones. An Unexpected Reaction Leading to 4,5-Polyalkylene Thiazoles

Barkoczy, Jozsef,Szabo, Eva,Reiter, Jozsef

, p. 1019 - 1024 (2007/10/02)

The reaction of 1,2,4-triazolylcarbothiohydrazides with homo- and heterocyclic ketones to yield 8-spirotriazolotetrazepine-5-thiones 7 (n = 4, 5, 6, 7 and 11), 8 and 9, respectively, all representing movel ring systems was studied.Providing the reaction at higher temperature a novel reaction was observed to yield 4,5-polyalkylene thiazoles for which a mechanism is proposed.

SYNTHESIS AND STRUCTURE OF LARGE RING 2-PHENYLCYCLOALKANONES AND 2,n-DIPHENYLCYCLOALKANONES

Lei, Xuegong,Doubleday, Charles,Turro, Nicholas J.

, p. 4671 - 4674 (2007/10/02)

The title compounds have been prepared in good yield by treating the corresponding 2,n-dibromocycloalkanone with LiCuPh2.Single-crystal X-ray structures are reported for cis- and trans-2,12-diphenylcyclododecanone.

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