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3,4-Dibromobenzoic acid ethyl ester, also known as Ethyl 3,4-dibromobenzoate, is an organic compound and a derivative of benzoic acid. It is characterized by its chemical structure that includes carbon, hydrogen, bromine, and oxygen atoms. 3,4-Dibromobenzoic acid ethyl ester is recognized for its reactivity and is often utilized in chemical research and various applications. It falls under the category of bromobenzoates and requires careful handling and appropriate safety measures due to its potential risks. The molecular weight of 3,4-Dibromobenzoic acid ethyl ester is 375.930 g/mol.

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  • 60469-88-7 Structure
  • Basic information

    1. Product Name: 3,4-DIBROMOBENZOIC ACID ETHYL ESTER
    2. Synonyms: ETHYL 3,4-DIBROMOBENZOATE;3,4-DIBROMOBENZOIC ACID ETHYL ESTER;RARECHEM AL BI 1504
    3. CAS NO:60469-88-7
    4. Molecular Formula: C9H8Br2O2
    5. Molecular Weight: 307.97
    6. EINECS: N/A
    7. Product Categories: Aromatic Esters;Acids & Esters;Bromine Compounds
    8. Mol File: 60469-88-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 331.7 °C at 760 mmHg
    3. Flash Point: 154.4 °C
    4. Appearance: /
    5. Density: 1.747 g/cm3
    6. Vapor Pressure: 0.000153mmHg at 25°C
    7. Refractive Index: 1.572
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 3,4-DIBROMOBENZOIC ACID ETHYL ESTER(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3,4-DIBROMOBENZOIC ACID ETHYL ESTER(60469-88-7)
    12. EPA Substance Registry System: 3,4-DIBROMOBENZOIC ACID ETHYL ESTER(60469-88-7)
  • 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: 60469-88-7(Hazardous Substances Data)

60469-88-7 Usage

Uses

Used in Chemical Research:
3,4-Dibromobenzoic acid ethyl ester is used as a research chemical for the investigation of its reactivity and potential applications in the field of chemistry. Its unique structure allows for the exploration of various chemical reactions and interactions.
Used in Pharmaceutical Industry:
3,4-Dibromobenzoic acid ethyl ester is used as an intermediate in the synthesis of pharmaceutical compounds. Its reactivity and structural properties make it a valuable component in the development of new drugs and medications.
Used in Material Science:
3,4-Dibromobenzoic acid ethyl ester is used as a component in the development of new materials with specific properties. Its chemical structure contributes to the creation of materials with tailored characteristics for various applications in material science.
Used in Environmental Applications:
3,4-Dibromobenzoic acid ethyl ester is used as a chemical in environmental remediation processes. Its reactivity can be harnessed to address specific environmental challenges, such as the treatment of contaminated water or soil.

Check Digit Verification of cas no

The CAS Registry Mumber 60469-88-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,6 and 9 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60469-88:
(7*6)+(6*0)+(5*4)+(4*6)+(3*9)+(2*8)+(1*8)=137
137 % 10 = 7
So 60469-88-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H8Br2O2/c1-2-13-9(12)6-3-4-7(10)8(11)5-6/h3-5H,2H2,1H3

60469-88-7Downstream Products

60469-88-7Relevant articles and documents

HIGH-AFFINITY CU(I) LIGANDS AND METHODS OF USE THEREOF

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Page/Page column 56-57, (2020/10/20)

Several dimethylphosphine sulfide- and phosphine-containing compounds have been discovered that chelate copper(I) with high affinity. In certain embodiments, the compounds can be used to quantify copper(I) in complex biological systems. In another embodim

Use of Potassium Bromate: Bromination of Halobenzenes and Halobenzoic Acids

Banerjee, Amalendu,Banerjee, Gopal Chandra,Dutt, Sachchidananda,Banerjee, Santa (Mrs.),Samaddar, Haraprasad

, p. 640 - 642 (2007/10/02)

Syntheses of bromo compounds by the bromination of halobenzenes and halobenzoic acids using potassium bromate under acidic condition have been discussed.

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