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2-BROMO-4,5-DIMETHOXYCINNAMIC ACID is a chemical compound belonging to the cinnamic acid family, characterized by the molecular formula C11H11BrO4. It features a cinnamic acid core with bromine and methoxy groups attached, which endows it with potential pharmaceutical applications, particularly in anti-inflammatory and anti-cancer properties. Its ability to inhibit cancer cell growth in laboratory settings positions it as a promising drug candidate for various cancer treatments.

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  • 151539-52-5 Structure
  • Basic information

    1. Product Name: 2-BROMO-4,5-DIMETHOXYCINNAMIC ACID
    2. Synonyms: LABOTEST-BB LT00455677;6-BROMO-3,4-DIMETHOXYCINNAMIC ACID;AKOS B005111;2-BROMO-4,5-DIMETHOXYCINNAMIC ACID;RARECHEM AL BK 0015
    3. CAS NO:151539-52-5
    4. Molecular Formula: C11H11BrO4
    5. Molecular Weight: 287.11
    6. EINECS: N/A
    7. Product Categories: Aromatic Cinnamic Acids, Esters and Derivatives
    8. Mol File: 151539-52-5.mol
  • Chemical Properties

    1. Melting Point: 253-259 °C
    2. Boiling Point: 409.5°Cat760mmHg
    3. Flash Point: 201.4°C
    4. Appearance: /
    5. Density: 1.517g/cm3
    6. Vapor Pressure: 1.94E-07mmHg at 25°C
    7. Refractive Index: 1.6
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. BRN: 3142451
    11. CAS DataBase Reference: 2-BROMO-4,5-DIMETHOXYCINNAMIC ACID(CAS DataBase Reference)
    12. NIST Chemistry Reference: 2-BROMO-4,5-DIMETHOXYCINNAMIC ACID(151539-52-5)
    13. EPA Substance Registry System: 2-BROMO-4,5-DIMETHOXYCINNAMIC ACID(151539-52-5)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 37/39-26
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 151539-52-5(Hazardous Substances Data)

151539-52-5 Usage

Uses

Used in Pharmaceutical Applications:
2-BROMO-4,5-DIMETHOXYCINNAMIC ACID is used as a drug candidate for its anti-inflammatory and anti-cancer properties, showing promise in inhibiting the growth of cancer cells in laboratory studies. It is being researched for its potential in treating various types of cancer.
Used in Organic Synthesis:
In the field of organic synthesis, 2-BROMO-4,5-DIMETHOXYCINNAMIC ACID is used as a building block for the preparation of various biologically active compounds, contributing to the development of new pharmaceuticals and other bioactive substances.

Check Digit Verification of cas no

The CAS Registry Mumber 151539-52-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,5,3 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 151539-52:
(8*1)+(7*5)+(6*1)+(5*5)+(4*3)+(3*9)+(2*5)+(1*2)=125
125 % 10 = 5
So 151539-52-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H11BrO4/c1-15-9-5-7(3-4-11(13)14)8(12)6-10(9)16-2/h3-6H,1-2H3,(H,13,14)/b4-3-

151539-52-5 Well-known Company Product Price

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  • Alfa Aesar

  • (A16862)  2-Bromo-4,5-dimethoxycinnamic acid, 97%   

  • 151539-52-5

  • 5g

  • 227.0CNY

  • Detail
  • Alfa Aesar

  • (A16862)  2-Bromo-4,5-dimethoxycinnamic acid, 97%   

  • 151539-52-5

  • 25g

  • 932.0CNY

  • Detail
  • Alfa Aesar

  • (A16862)  2-Bromo-4,5-dimethoxycinnamic acid, 97%   

  • 151539-52-5

  • 100g

  • 3187.0CNY

  • Detail

151539-52-5SDS

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 3-(2-bromo-4,5-dimethoxyphenyl)prop-2-enoic acid

1.2 Other means of identification

Product number -
Other names 6-Brom-3.4-dimethoxy-trans-zimtsaeure

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:151539-52-5 SDS

151539-52-5Relevant articles and documents

Competitive formation of β-amino acids, propenoic, and ylidenemalonic acids by the Rodionov reaction from malonic acid, aldehydes, and ammonium acetate in alcoholic medium

Lebedev,Lebedeva,Sheludyakov,Kovaleva,Ustinova,Kozhevnikov

, p. 1113 - 1124 (2007/10/03)

The Rodionov reaction of 49 available aliphatic and aromatic aldehydes with malonic acid and ammonium acetate in alcoholic medium, resulting in formation of β-amino acids, propenoic, and ylidenemalonic acids, was studied. Certain regioselectivity regularities of the reaction were revealed. Among the variety of ketones studied, cyclohexanone is the only whose reaction yields a β-amino acid. Unusual dehydrofluorination of 6-chloro-2-fluorocinnamic acid under the Rodionov reaction was discovered. 2005 Pleiades Publishing, Inc.

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