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CAS

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112930-39-9

3-Bromo-5-isopropylbenzoic acid is a chemical compound with the molecular formula C10H11BrO2, belonging to the benzoic acid derivatives. It features a bromine atom and an isopropyl group attached to the benzene ring, which endows it with unique chemical properties and potential applications in various fields.

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  • 112930-39-9 Structure

  • Basic information

    1. Product Name: 3-Bromo-5-isopropylbenzoic acid
    2. Synonyms: 3-Bromo-5-isopropylbenzoic acid;3-bromo-5-propan-2-ylbenzoic acid
    3. CAS NO:112930-39-9
    4. Molecular Formula: C10H11BrO2
    5. Molecular Weight: 243.09714
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 112930-39-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 329.5±35.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.445±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. PKA: 3.85±0.10(Predicted)
    10. CAS DataBase Reference: 3-Bromo-5-isopropylbenzoic acid(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-Bromo-5-isopropylbenzoic acid(112930-39-9)
    12. EPA Substance Registry System: 3-Bromo-5-isopropylbenzoic acid(112930-39-9)

  • 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: 112930-39-9(Hazardous Substances Data)

112930-39-9 Usage

Uses

Used in Pharmaceutical Synthesis:
3-Bromo-5-isopropylbenzoic acid is used as an intermediate in the synthesis of pharmaceuticals for its ability to serve as a building block for the development of diverse organic compounds. Its presence in the structure of target molecules can contribute to the desired therapeutic effects.
Used in Agrochemical Production:
In the agrochemical industry, 3-Bromo-5-isopropylbenzoic acid is utilized as an intermediate in the production of various agrochemicals, potentially enhancing the effectiveness of these products in agricultural applications.
Used in Organic Chemistry Research:
3-Bromo-5-isopropylbenzoic acid is used as a valuable building block in organic chemistry for the synthesis of a wide range of organic compounds, facilitating the exploration of new chemical reactions and the creation of novel molecules.
Used in Anti-Inflammatory and Antimicrobial Studies:
3-Bromo-5-isopropylbenzoic acid is studied for its potential anti-inflammatory and antimicrobial properties, which could lead to its use in the development of new treatments for inflammation and infections.
Overall, 3-Bromo-5-isopropylbenzoic acid holds significant potential across the fields of medicine, pharmaceuticals, and organic chemistry, making it a versatile compound for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 112930-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,3 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112930-39:
(8*1)+(7*1)+(6*2)+(5*9)+(4*3)+(3*0)+(2*3)+(1*9)=99
99 % 10 = 9
So 112930-39-9 is a valid CAS Registry Number.

112930-39-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-5-propan-2-ylbenzoic acid

1.2 Other means of identification

Product number -
Other names 3-Bromo-5-isopropylbenzoic 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:112930-39-9 SDS

112930-39-9Upstream product

112930-39-9Relevant articles and documents

Steric Effects. Internal Rotation of 1-Aryl-8-phenylnaphthalenes

Cosmo, Robert,Sternhell, Sever

, p. 1107 - 1126 (2007/10/02)

A general, albeit low-yielding, synthesis of 1-aryl-8-phenylnaphthalenes was devised and used to prepare three 1-(3'-X-5'-isopropylphenyl)-8-phenylnaphthalenes (X = H, F, Br).Activation parameters for the rotation of the 3'-X-5'-isopropylphenyl group were

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