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260365-89-7

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260365-89-7 Usage

Description

9-(Iodomethyl)anthracene is a chemical compound that consists of an anthracene molecule with a methyl group and an iodine atom attached to one of the carbon atoms. It is characterized by its potential reactivity and the presence of the iodine atom, which makes it useful in various chemical reactions, particularly in the formation of carbon-carbon bonds.

Uses

Used in Organic Synthesis:
9-(Iodomethyl)anthracene is used as a fluorescent labeling reagent for the purpose of tracking and identifying specific molecules in organic synthesis processes. Its fluorescent properties allow for easy detection and analysis.
Used in Pharmaceutical Manufacturing:
In the pharmaceutical industry, 9-(Iodomethyl)anthracene serves as a precursor in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity contribute to the development of new drugs and medicinal agents.
Used in Dye Production:
9-(Iodomethyl)anthracene is utilized as a starting material in the production of dyes. Its chemical properties make it suitable for creating a range of dyes with specific color characteristics and applications.
Used in Chemical Research:
Due to its reactivity and the presence of the iodine atom, 9-(Iodomethyl)anthracene is used in chemical research to study and develop new methods for forming carbon-carbon bonds and other chemical reactions.
Safety and Handling:

Check Digit Verification of cas no

The CAS Registry Mumber 260365-89-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,0,3,6 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 260365-89:
(8*2)+(7*6)+(6*0)+(5*3)+(4*6)+(3*5)+(2*8)+(1*9)=137
137 % 10 = 7
So 260365-89-7 is a valid CAS Registry Number.

260365-89-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-(Iodomethyl)anthracene

1.2 Other means of identification

Product number -
Other names Anthracene,9-(iodomethyl)

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:260365-89-7 SDS

260365-89-7Relevant articles and documents

Silicaphosphine (Silphos): A filterable reagent for the conversion of alcohols and thiols to alkyl bromides and iodides

Iranpoor, Nasser,Firouzabadi, Habib,Jamalian, Arezu,Kazemi, Foad

, p. 5699 - 5704 (2007/10/03)

Silicaphosphine (Silphos), [P(Cl)3-n(SiO2) n], as a new heterogeneous reagent is introduced. This reagent converts alcohols and thiols to their corresponding bromides and iodides in the presence of X2 (X=Br, I) in refluxing CH3CN in high to quantitative yields. Use of Silphos provides a highly practical method for the easy separation of the Silphos oxide byproduct by a simple filtration.

An easy synthesis of lepidopterene from 9-chloromethyl anthracene. Evidence for a free radical mechanism

Fernández, María-José,Gude, Lourdes,Lorente, Antonio

, p. 891 - 893 (2007/10/03)

This communication reports a novel and efficient synthesis of lepidopterene from 9-(chloromethyl)anthracene. Furthermore, the radical nature of the process is unambiguously established through the obtention of several 9-anthracenemethyl derivatives, which are formed via a common 9-anthracenemethyl radical intermediate, derived from 9-(iodomethyl)anthracene.

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