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696-41-3

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696-41-3 Usage

Description

3-Iodobenzaldehyde is an organic compound with the chemical formula C6H4(I)CHO, featuring a benzene ring with an aldehyde group at the 3-position and an iodine atom attached to the same carbon. It is a pale yellow crystalline powder that can be synthesized through the iodination of benzaldehyde using 1,3-diiodo-5,5-dimethylhydantoin in sulfuric acid.

Uses

Used in Organic Synthesis:
3-Iodobenzaldehyde is used as an organic reagent for various chemical reactions and synthesis processes. Its unique structure with both an iodine atom and an aldehyde group allows it to participate in a wide range of reactions, making it a versatile building block in organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Iodobenzaldehyde is used as a key intermediate in the synthesis of various drugs and pharmaceutical compounds. Its reactivity and structural properties make it a valuable component in the development of new medications.
Used in Chemical Research:
3-Iodobenzaldehyde is also utilized in academic and industrial research settings for studying chemical reactions and exploring new synthetic pathways. Its unique properties and reactivity contribute to the advancement of knowledge in the field of chemistry.
Used in Material Science:
In the field of material science, 3-Iodobenzaldehyde can be employed in the development of novel materials with specific properties, such as optoelectronic materials or advanced polymers, due to its ability to undergo various chemical transformations.
Overall, 3-Iodobenzaldehyde is a valuable compound with diverse applications across different industries, including organic synthesis, pharmaceuticals, chemical research, and material science, thanks to its unique chemical properties and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 696-41-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 696-41:
(5*6)+(4*9)+(3*6)+(2*4)+(1*1)=93
93 % 10 = 3
So 696-41-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H5IO/c8-7-3-1-2-6(4-7)5-9/h1-5H

696-41-3 Well-known Company Product Price

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  • Alfa Aesar

  • (L17447)  3-Iodobenzaldehyde, 98%   

  • 696-41-3

  • 1g

  • 854.0CNY

  • Detail
  • Alfa Aesar

  • (L17447)  3-Iodobenzaldehyde, 98%   

  • 696-41-3

  • 5g

  • 3572.0CNY

  • Detail

696-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Iodobenzaldehyde

1.2 Other means of identification

Product number -
Other names 3-Jod-benzaldehyd

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:696-41-3 SDS

696-41-3Relevant articles and documents

Unprecedented Halide-Ion Binding and Catalytic Activity of Nanoscale Anionic Metal Oxide Clusters

She, Shan,Li, Mu,Li, Qi,Huang, Zehuan,Wei, Yongge,Yin, Panchao

, p. 1668 - 1672 (2019)

One halide ion (X?) can bind on the surface of nanoscale Anderson-type polyoxometalate (POMs) clusters [(n-C4H9)4N]3{AlMo6O18(OH)3[(OCH2)3CCH3]}, and form stable complexes in solution with binding constant K=1.53×103. Single-crystal structural analysis showed that this binding behavior occurs through multiple hydrogen bonding between X? and three hydroxy groups on the uncapped side of the cluster. This supramolecular interaction in the cluster systems means that their catalytic activities, evaluated from the oxidation of alcohols to aldehydes, can be switched upon the introduction of halide ions and water molecules. The halide ions work as inhibitors by blocking the active sites of the clusters while they can be re-activated by the addition of water.

V2O5@TiO2 Catalyzed Green and Selective Oxidation of Alcohols, Alkylbenzenes and Styrenes to Carbonyls

Upadhyay, Rahul,Kumar, Shashi,Maurya, Sushil K.

, p. 3594 - 3600 (2021/07/02)

The versatile application of different functional groups such as alcohols (1° and 2°), alkyl arenes, and (aryl)olefins to construct carbon-oxygen bond via oxidation is an area of intense research. Here, we report a reusable heterogeneous V2O5@TiO2 catalyzed selective oxidation of various functionalities utilizing different mild and eco-compatible oxidants under greener reaction conditions. The method was successfully applied for the alcohol oxidation, oxidative scission of styrenes, and benzylic C?H oxidation to their corresponding aldehydes and ketones. The utilization of mild and eco-friendly oxidizing reagents such as K2S2O8, H2O2 (30 % aq.), TBHP (70 % aq.), broad substrate scope, gram-scale synthesis, and catalyst recyclability are notable features of the developed protocol.

AN IMPROVED ONE POT, ONE STEP PROCESS FOR THE HALOGENATION OF AROMATICS USING SOLID ACID CATALYSTS

-

Page/Page column 0047; 0048, (2019/04/18)

The present invention disclosed an improved one pot, one step process for halogenation of compound of formula (II) to afford corresponding halogenated compound of formula (I) having improved yield and increased selectivity under very mild conditions.

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