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2-HYDROXY-5-IODO-4-METHYLBENZOIC ACID is a chemical compound with the molecular formula C8H7IO3, belonging to the benzoic acid derivatives. It features a hydroxyl group and an iodo group on the benzene ring, which endows it with unique chemical properties. 2-HYDROXY-5-IODO-4-METHYLBENZOIC ACID is recognized for its role as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and its versatile chemical structure and properties make it a valuable building block in organic synthesis and medicinal chemistry.

850146-83-7

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850146-83-7 Usage

Uses

Used in Pharmaceutical Industry:
2-HYDROXY-5-IODO-4-METHYLBENZOIC ACID is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic applications. Its unique structure allows for the creation of molecules with specific biological activities, making it a key component in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 2-HYDROXY-5-IODO-4-METHYLBENZOIC ACID is utilized as an intermediate in the production of agrochemicals, contributing to the development of effective and targeted pest control agents. Its chemical properties facilitate the design of compounds that can be selectively toxic to pests while being safer for the environment.
Used in Dye Production:
2-HYDROXY-5-IODO-4-METHYLBENZOIC ACID is used as a building block in the production of dyes due to its chemical structure that can be modified to produce a range of colors. Its versatility in synthesis allows for the creation of dyes with specific properties, such as lightfastness and resistance to fading, which are important in various industries including textiles and printing.
Used in Organic Synthesis:
As a versatile organic compound, 2-HYDROXY-5-IODO-4-METHYLBENZOIC ACID is used in organic synthesis for the preparation of other organic compounds. Its reactivity and functional groups make it a suitable candidate for further chemical reactions, leading to the formation of a wide array of molecules with diverse applications in research and industry.

Check Digit Verification of cas no

The CAS Registry Mumber 850146-83-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,1,4 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 850146-83:
(8*8)+(7*5)+(6*0)+(5*1)+(4*4)+(3*6)+(2*8)+(1*3)=157
157 % 10 = 7
So 850146-83-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H7IO3/c1-4-2-7(10)5(8(11)12)3-6(4)9/h2-3,10H,1H3,(H,11,12)

850146-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxy-5-iodo-4-methylbenzoic acid

1.2 Other means of identification

Product number -
Other names 2-Hydroxy-5-jod-4-methyl-benzoesaeure

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:850146-83-7 SDS

850146-83-7Relevant academic research and scientific papers

Potassium 4-iodylbenzenesulfonate: Preparation, structure, and application as a reagent for oxidative iodination of arenes

Yusubov, Mekhman S.,Yusubova, Roza Y.,Nemykin, Victor N.,Maskaev, Andrey V.,Geraskina, Margarita R.,Kirschning, Andreas,Zhdankin, Viktor V.

, p. 5935 - 5942,8 (2020/09/02)

A new hypervalent iodine(V) compound, potassium 4-iodylbenzenesulfonate, was prepared by the oxidation of 4-iodobenzensulfonic acid with Oxone in water. This potassium salt can be further converted into 4-iodylbenzenesulfonic acid by treatment with the acidic form of Amberlyst 15 in water. A single-crystal X-ray structure of potassium 4-iodylbenzenesulfonate revealed the presence of polymeric chains in the solid state due to a combination of numerous intra- and intermolecular interactions. Potassium 4-iodylbenzenesulfonate will likely find many practical applications as a thermally stable and water-soluble hypervalent iodine-based oxidant, particularly useful as a reagent for oxidative iodination of aromatic substrates. This reagent can be effectively recovered from the reaction mixture (92 % recovery) by treatment of the aqueous layer with Oxone at 60°C for 2 h, followed by filtration of the precipitate. A new hypervalent iodine(V) compound, potassium 4-iodylbenzenesulfonate, was prepared by oxidation of 4-iodobenzenesulfonic acid with Oxone in water. This new reagent promises many practical applications as a thermally stable, water-soluble and recyclable hypervalent iodine oxidant, particularly useful for oxidative iodination of aromatic substrates.

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