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4-IODO-2-METHOXYBENZOIC ACID, with the molecular formula C8H7IO3, is a benzoic acid derivative characterized by the presence of both an iodo and a methoxy group. This chemical compound is recognized for its unique structure and reactivity, which positions it as a valuable asset in the realm of medicinal chemistry and drug development.

89942-34-7

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89942-34-7 Usage

Uses

Used in Organic Synthesis:
4-IODO-2-METHOXYBENZOIC ACID is used as an intermediate in organic synthesis for its distinctive properties and reactivity, contributing to the creation of various chemical products.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 4-IODO-2-METHOXYBENZOIC ACID is utilized as a building block for the production of pharmaceuticals, playing a crucial role in the development of new drugs.
Used in Medicinal Chemistry:
4-IODO-2-METHOXYBENZOIC ACID is employed as a valuable tool in medicinal chemistry, where its unique structure aids in the design and synthesis of potential therapeutic agents.
Used in Drug Development:
4-IODO-2-METHOXYBENZOIC ACID is also used in drug development, where its distinctive properties are leveraged to enhance the efficacy and safety of new pharmaceuticals.
Used in the Development of New Materials:
4-IODO-2-METHOXYBENZOIC ACID has potential applications in the development of new materials, capitalizing on its distinctive chemical properties to innovate in material science.
Used in Chemical Processes:
4-IODO-2-METHOXYBENZOIC ACID is also utilized in the development of new chemical processes, where its reactivity and unique structure can lead to more efficient or novel methods in chemical engineering.

Check Digit Verification of cas no

The CAS Registry Mumber 89942-34-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,9,4 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89942-34:
(7*8)+(6*9)+(5*9)+(4*4)+(3*2)+(2*3)+(1*4)=187
187 % 10 = 7
So 89942-34-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H7IO3/c1-12-7-4-5(9)2-3-6(7)8(10)11/h2-4H,1H3,(H,10,11)

89942-34-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Iodo-2-methoxybenzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid,4-iodo-2-methoxy

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:89942-34-7 SDS

89942-34-7Relevant academic research and scientific papers

Novel tricyclic pyridyl carboxamides and derivatives thereof tocolytic oxytocin receptor antagonists

-

, (2008/06/13)

This invention provides novel substituted tricyclic pyridyl carboxamides which act as oxytocin receptor competitive antagonists, as well as methods of their manufacture, pharmaceutical compositions and methods of their use in treatment, inhibition, suppression or prevention of preterm labor, dysmenorrhea, endometritis, suppression of labor at term prior to caesarean delivery, and to facilitate antinatal transport to a medical facility. These compounds are also useful in enhancing fertility rates, enhancing survival rates and synchronizing estrus in farm animals; and may be useful in the prevention and treatment of disfunctions of the oxytocin system in the central nervous system including obsessive compulsive disorder (OCD) and neuropsychiatric disorders.

Kinetics of Iodination of Some Substituted Benzoic Acids by N-Iodosuccinimide

Radhakrishnamurti, P. S.,Panda, B. K.

, p. 770 - 773 (2007/10/02)

Iodination of o-amino-, p-amino-, o-hydroxy-, p-hydroxy, o-acetylamino-, p-acetylamino-, o-methoxy- and p-methoxy-benzoic acids by N-iodosuccinimide (NIS) in mixtures of acetic acid and perchloric acid follows first order kinetics with respect to the halo

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