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CAS

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133232-58-3

4-iodo-2-Methylbenzoic acid is an organic compound with the chemical formula C8H7IO3. It is a derivative of benzoic acid, featuring a methyl group at the 2nd position and an iodine atom at the 4th position on the benzene ring. 4-iodo-2-Methylbenzoic acid is known for its potential applications in various fields, particularly in the pharmaceutical and chemical industries.

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  • 133232-58-3 Structure

  • Basic information

    1. Product Name: 4-iodo-2-Methylbenzoic acid
    2. Synonyms: 4-iodo-2-Methylbenzoic acid
    3. CAS NO:133232-58-3
    4. Molecular Formula: C8H7IO2
    5. Molecular Weight: 262.04445
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133232-58-3.mol

  • Chemical Properties

    1. Melting Point: 172 °C(Solv: water (7732-18-5))
    2. Boiling Point: 326.5±30.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.867±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: -20°C Freezer, Under inert atmosphere
    8. Solubility: Aqueous Base (Slightly), Chloroform (Slightly), DMSO (Slightly)
    9. PKA: 3.70±0.25(Predicted)
    10. CAS DataBase Reference: 4-iodo-2-Methylbenzoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 4-iodo-2-Methylbenzoic acid(133232-58-3)
    12. EPA Substance Registry System: 4-iodo-2-Methylbenzoic acid(133232-58-3)

  • 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: 133232-58-3(Hazardous Substances Data)

133232-58-3 Usage

Uses

Used in Pharmaceutical Industry:
4-iodo-2-Methylbenzoic acid is used as a 15-PGDH inhibitor for preventing and treating 15-PGDH-related diseases. It targets the 15-PGDH pathway, which plays a crucial role in various physiological processes, including fibrosis, inflammation, cardiovascular disease, wound healing, and auto-immune diseases. By inhibiting this pathway, 4-iodo-2-Methylbenzoic acid can help manage and alleviate the symptoms associated with these conditions.
Used in Chemical Industry:
In the chemical industry, 4-iodo-2-Methylbenzoic acid can be utilized as a building block or intermediate in the synthesis of various organic compounds and pharmaceuticals. Its unique structure, featuring both a methyl and an iodine substituent, makes it a valuable component in the development of new molecules with specific properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 133232-58-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,2,3 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 133232-58:
(8*1)+(7*3)+(6*3)+(5*2)+(4*3)+(3*2)+(2*5)+(1*8)=93
93 % 10 = 3
So 133232-58-3 is a valid CAS Registry Number.

133232-58-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Iodo-2-methylbenzoic acid

1.2 Other means of identification

Product number -
Other names 4-Iod-2-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:133232-58-3 SDS

133232-58-3Relevant articles and documents

Doxepin analogs and methods of use thereof

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Page/Page column 51, (2008/06/13)

The invention relates to novel antihistamines and methods of modulating sleep by administering a doxepin analog or a pharmaceutically effective salt thereof.

Aryl and heteroaryl (phosphinylmethyl)phosphonate squalene synthetase inhibitors and method

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, (2008/06/13)

Phosphonic acid squalene synthetase inhibitors are provided which are effective in lowering serum cholesterol and have the formula STR1 wherein m is 0 to 3, n is 1 to 5, Y1 and Y2 are H or halogen, R2, R3 and R4 are H, metal ion, C1 to C8 alkyl, C3 to C12 alkenyl, or prodrug ester, and R1 is a substituted or unsubstituted heteroaryl group or a substituted phenyl group.

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