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CAS

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294860-98-3

(5-iodo-2-methoxyphenyl)acetic acid is a chemical compound with the molecular formula C9H9IO3, derived from acetic acid and featuring a substituted phenyl ring with an iodine atom and a methoxy group. It has been investigated for its potential pharmaceutical properties, particularly as an anti-inflammatory and analgesic agent, and is believed to work by inhibiting the production of prostaglandins, which are involved in the inflammatory response. (5-iodo-2-methoxyphenyl)acetic acid's structure and properties make it a potentially valuable building block for the synthesis of novel pharmaceutical compounds.

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  • 294860-98-3 Structure

  • Basic information

    1. Product Name: (5-iodo-2-methoxyphenyl)acetic acid
    2. Synonyms: (5-iodo-2-methoxyphenyl)acetic acid;5-iodo-2-methoxyBenzeneacetic acid
    3. CAS NO:294860-98-3
    4. Molecular Formula: C9H9IO3
    5. Molecular Weight: 292.07
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 294860-98-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (5-iodo-2-methoxyphenyl)acetic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (5-iodo-2-methoxyphenyl)acetic acid(294860-98-3)
    11. EPA Substance Registry System: (5-iodo-2-methoxyphenyl)acetic acid(294860-98-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 294860-98-3(Hazardous Substances Data)

294860-98-3 Usage

Uses

Used in Pharmaceutical Industry:
(5-iodo-2-methoxyphenyl)acetic acid is used as an anti-inflammatory and analgesic agent for its ability to inhibit the production of prostaglandins, which are involved in the inflammatory response. This makes it a promising candidate for the development of new drugs targeting inflammation and pain.
Used in Drug Synthesis:
(5-iodo-2-methoxyphenyl)acetic acid is used as a building block for the synthesis of novel pharmaceutical compounds due to its unique structure and properties. Its potential applications in the development of new drugs are currently being explored through ongoing research.

Check Digit Verification of cas no

The CAS Registry Mumber 294860-98-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,4,8,6 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 294860-98:
(8*2)+(7*9)+(6*4)+(5*8)+(4*6)+(3*0)+(2*9)+(1*8)=193
193 % 10 = 3
So 294860-98-3 is a valid CAS Registry Number.

294860-98-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-iodo-2-methoxyphenyl)acetic acid

1.2 Other means of identification

Product number -
Other names (5-iodo-2-methoxyphenyl)acetate

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:294860-98-3 SDS

294860-98-3Relevant articles and documents

Palladium-catalyzed meta-C[sbnd]H bond iodination of arenes with I2

Liu, Min,Li, Ling-Jun,Zhang, Jun,Xu, Hui,Dai, Hui-Xiong

, p. 1301 - 1304 (2020)

Palladium-catalyzed highly meta-selective C[sbnd]H iodination of phenylacetic acid, benzylphosphonate and benzylsulfonate scaffolds with molecular I2 is developed using a pyridine-type template. The practical ester linkages enable the directing template easily installed and readily removed. The substrate scope is broad, and alkyl, methoxyl, trifluomethyl, and halo substituents are compatible with this reaction. Further transformations of ibuprofen iodide intermediates by Pd-catalyzed C[sbnd]C and C–heteroatom bond formation illustrate the broad utility of this method.

IRREVERSIBLE CASPASE-3 INHIBITORS AS ACTIVE SITE PROBES

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Page 24, (2008/06/13)

The present invention encompasses a compound of Formula (I) useful as caspase active site probes. These probes can be used to determine whether a caspase has been activated, in cells or in tissues of animal models of various pathologies. Furthermore, thro

CHROMANES AND THEIR PHARMACEUTICAL COMPOSITIONS AND METHODS

-

, (2008/06/13)

Racemic Compounds of the formula I and their enantiomer and salts thereof are described. The compounds of formula I exhibit activity as inhibitors of 5-lipoxygenase and inhibit lipid peroxidation. They are, therefore, useful in the treatment of diseases caused or aggravated by excess oxidative metabolism of arachidonic acid via the 5-lipoxygenase pathway and in the treatment of inflammation, arthritis, allergies, asthma and psoriasis. The compounds of formula I can also be used to prevent peroxidation of lipids and thus protect lipid membranes from oxidative stress

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