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CAS

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94232-67-4

2-[4-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)phenyl]butyric acid is a chemical compound that is a derivative of Indobufen, a platelet aggregation inhibitor and anticoagulant drug with anti-inflammatory and analgesic effects.

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  • Benzeneacetic acid, 4-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-a-ethyl-

    Cas No: 94232-67-4

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  • 94232-67-4 Structure

  • Basic information

    1. Product Name: 2-[4-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)phenyl]butyric acid
    2. Synonyms: 2-[4-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)phenyl]butyric acid;α-Ethyl-4-[(1,3-dihydro-1,3-dioxo-2H-isoindol)-2-yl]benzeneacetic acid;Indobufen Impurity 10
    3. CAS NO:94232-67-4
    4. Molecular Formula: C18H15NO4
    5. Molecular Weight: 309.316
    6. EINECS: 303-995-2
    7. Product Categories: N/A
    8. Mol File: 94232-67-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 527.9°Cat760mmHg
    3. Flash Point: 273.1°C
    4. Appearance: /
    5. Density: 1.356g/cm3
    6. Vapor Pressure: 5.67E-12mmHg at 25°C
    7. Refractive Index: 1.643
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. Water Solubility: 7.72mg/L at 20℃
    11. CAS DataBase Reference: 2-[4-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)phenyl]butyric acid(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-[4-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)phenyl]butyric acid(94232-67-4)
    13. EPA Substance Registry System: 2-[4-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)phenyl]butyric acid(94232-67-4)

  • 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: 94232-67-4(Hazardous Substances Data)

94232-67-4 Usage

Uses

Used in Pharmaceutical Industry:
2-[4-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)phenyl]butyric acid is used as an antithrombotic agent for the prevention and treatment of thrombotic disorders, such as deep vein thrombosis, pulmonary embolism, and myocardial infarction. Its ability to inhibit platelet aggregation and reduce blood clot formation makes it a valuable compound in the development of antithrombotic medications.

Flammability and Explosibility

Notclassified

Check Digit Verification of cas no

The CAS Registry Mumber 94232-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,2,3 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 94232-67:
(7*9)+(6*4)+(5*2)+(4*3)+(3*2)+(2*6)+(1*7)=134
134 % 10 = 4
So 94232-67-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H15NO4/c1-2-13(18(22)23)11-7-9-12(10-8-11)19-16(20)14-5-3-4-6-15(14)17(19)21/h3-10,13H,2H2,1H3,(H,22,23)

94232-67-4SDS

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-[4-(1,3-dioxoisoindol-2-yl)phenyl]butanoic acid

1.2 Other means of identification

Product number -
Other names 2-(4-(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)phenyl)butyric acid

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:94232-67-4 SDS

94232-67-4Downstream Products

94232-67-4Relevant articles and documents

Method for preparing indobufen

-

Paragraph 0028; 0029; 0031; 0032; 0033, (2017/08/29)

The invention discloses a method for preparing indobufen; by optimizing the processes such as using a carbon-supported noble metal as a catalyst in hydrogenation reduction, using a suitable organic acid solvent in zinc powder reduction and introducing hydrogen chloride gas, the preparation method of indobufen is simple to perform and high in yield; the whole preparation method is good in safety, environmentally friendly, good for protecting the health of workers and suitable for industrial use, and the purity of prepared indobufen is high.

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