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3,5-Diiodobenzyl alcohol, with the molecular formula C7H6I2O, is a colorless to pale yellow liquid compound. It features a benzyl alcohol group with two iodine atoms attached, which contributes to its reactivity and capacity for diverse chemical reactions. This characteristic makes it a valuable building block in organic synthesis for the preparation of a range of organic compounds.

53279-79-1

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53279-79-1 Usage

Uses

Used in Organic Synthesis:
3,5-Diiodobenzyl alcohol is used as a building block in organic synthesis for the preparation of various organic compounds due to its reactivity and ability to participate in multiple chemical reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3,5-Diiodobenzyl alcohol is utilized as a raw material for the synthesis of potential drug candidates, capitalizing on its chemical properties to contribute to the development of new medicinal compounds.
Used in Preparation of Functional Materials:
3,5-Diiodobenzyl alcohol is also employed in the preparation of functional materials, highlighting its versatility and importance in the field of organic chemistry for creating materials with specific applications.
Used in Fine Chemicals Production:
3,5-Diiodobenzyl alcohol is further used in the production of fine chemicals, where its unique structure and reactivity are leveraged to produce high-quality specialty chemicals for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 53279-79-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,2,7 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53279-79:
(7*5)+(6*3)+(5*2)+(4*7)+(3*9)+(2*7)+(1*9)=141
141 % 10 = 1
So 53279-79-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H6I2O/c8-6-1-5(4-10)2-7(9)3-6/h1-3,10H,4H2

53279-79-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3,5-diiodophenyl)methanol

1.2 Other means of identification

Product number -
Other names Benzenemethanol,3,5-diiodo

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:53279-79-1 SDS

53279-79-1Relevant articles and documents

A novel photoaffinity probe for the LTD4 receptor

Gallant, Michel,Sawyer, Nicole,Metters, Kathleen M.,Zamboni, Robert J.

, p. 63 - 72 (1998)

A novel photoaffinity probe for the leukotriene D4 receptor (LTD4) is described. L-745310, which is structurally related to the potent LTD4 antagonist MK-0476 (Singulair(TM)), was found to selectively label a 43-kDa protei

A rigid metallohexameric macrocycle composed of endo- and exo-cyclic bisterpyridine-metal complexes

Li, Sinan,Moorefield, Charles N.,Shreiner, Carol D.,Wang, Pingshan,Sarkar, Rajarshi,Newkome, George R.

experimental part, p. 2130 - 2135 (2011/11/13)

Synthesis of terpyridine-based building blocks has allowed the self-assembly of a nanosized metallomacrocycle with precisely positioned, peripheral metal complexes. Construction of the precursors included the assembly of a heteroleptic bisterpyridine-Ru(ii) complex possessing a diiodoaryl moiety that was subsequently reacted with two equivalents of 4′-ethynyl-2, 2′:6′,2′′-terpyridine via a Pd(0)-catalyzed Sonagashira coupling, to generate the requisite monomer with two, 120°-juxtaposed metal coordination sites. Addition of one equivalent of Fe(ii) to one equivalent of the bisligand afforded the metallocycle with 12 metals [6 internal Fe(ii) ions and 6 external Ru(ii) ions] measuring ca. 7 nm in diameter.

Conjugated oligoyne-bridged [60]fullerene molecular dumbbells: Syntheses and thermal and morphological properties

Zhou, Ningzhang,Zhao, Yuming

experimental part, p. 1498 - 1516 (2010/05/02)

Chemical Equation Presented A series of linear and star-shaped π-conjugated oligomer hybrids (2-5) composed of an oligoyne core, ranging from 1,3-butadiyne to 1,3,5,7,9,11-dodecahexayne, and fullerenyl end-capping groups has been synthesized and studied.

Solid-phase approaches toward cyclic oligomers

Shortell, David B.,Palmer, Liam C.,Tour, James M.

, p. 9055 - 9065 (2007/10/03)

Strategies were sought to effect cyclizations of oligo(m-phenylene ethynylene) by exploiting pseudo-high dilution effects on polymer supports. Using Pd/Cu-catalyzed coupling protocols, Merrifield's resin (1% crosslinked chloromethylated polystyrene) proved inadequate for site isolation; inter-site couplings ensued on the flexible support. Conversely, use of the Argopore resin, a more highly crosslinked polystyrene, inhibited inter-site interactions, and no identifiable final product could be separated from the resin. Spectroscopic and mass spectrometric methods indicated that the product from the Argopore resin might be a threaded catenane.

Synthetic studies on dendritic glycoclusters: A convergent palladium-catalyzed strategy

Sengupta, Saumitra,Sadhukhan, Subir Kumar

, p. 215 - 219 (2007/10/03)

A facile Pd-catalyzed strategy by which multiantennary glycoclusters and sugar dendrons can be readily assembled in one-step is described.

Iodo-aryl carbonates for use in methods in radiography

-

, (2008/06/13)

A method for using iodo-aryl carbonates, such as for example, p-iodo-benzyl carbonates, p-iodo-sec-phenethyl carbonates, p-iodo-phenethyl carbonates, p-iodo-phenyl carbonates, 3-(p-iodophenyl)propyl carbonates, 3-(p-iodophenyl)butyl carbonates, 2-(p-iodobenzyl)butyl carbonates and 2-(p-iodobenzyl)-n-hexyl carbonates, to provide radiopaques for various radiography purposes in connection with such techniques as X-ray applications including myelography, salpingography, lymphography and bronchography. The method first comprises selecting a compound generally categorized as a carbonate and having the general formula STR1 wherein R represents an alkyl group having from 1 to 10 carbon atoms and R' represents an iodinated phenyl linked directly to the ester oxygen or through an alkyl chain consisting of 1 to 3 carbon atoms. An effective amount of a pharmaceutically acceptable carbonate, as defined herein, is then placed into the subject body cavity and the particular X-ray or other study performed of this area.

Iodine containing organic carbonates for use as radiographic agents

-

, (2008/06/13)

Iodo-aryl carbonates, such as for example, p-iodo-benzyl carbonates, p-iodo-sec-phenethyl carbonates, p-iodo-phenethyl carbonates, p-iodo-phenyl carbonates, 3-(p-iodophenyl)propyl carbonates, 3-(p-iodophenyl)butyl carbonates, 2-(p-iodobenzyl)butyl carbonates and 2-(p-iodobenzyl)-n-hexyl carbonates, for use as radiographic media in connection with such techniques as x-ray applications including myelography, salpingography, lymphography and bronchography. An effective quantity of iodinated organic carbonate provides x-ray contrast, and the compounds of the invention may be characterized generally as carbonates having the general formula STR1 wherein R represents an alkyl group having from 4 to 10 carbon atoms and R' represents an iodinated phenyl linked to the ester oxygen through an alkyl chain consisting of 1 to 3 carbon atoms.

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