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2-(4-BROMOPHENYL)MALONDIALDEHYDE, with the chemical formula C9H6BrO2, is a yellow crystalline solid that features a benzene ring with a bromine substituent and two adjacent aldehyde groups on the malondialdehyde backbone. This chemical compound is frequently utilized as a precursor in the synthesis of a variety of organic compounds and holds promise in the realm of medicinal chemistry due to its structural properties.

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  • 709648-68-0 Structure
  • Basic information

    1. Product Name: 2-(4-BROMOPHENYL)MALONDIALDEHYDE
    2. Synonyms: 2-(4-BROMPHENYL)MALONDIALDEHYDE;2-(4-BROMOPHENYL)MALONDIALDEHYDE;(4-broMophenyl)Malondialdehyde;2-(4-Bromophenyl)malonaldehyde;2-(4-Bromophenyl)propane-1,3-dial
    3. CAS NO:709648-68-0
    4. Molecular Formula: C9H7BrO2
    5. Molecular Weight: 227.05
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 709648-68-0.mol
  • Chemical Properties

    1. Melting Point: 157-160
    2. Boiling Point: 302.3 °C at 760 mmHg
    3. Flash Point: 111.1 °C
    4. Appearance: /
    5. Density: 1.51 g/cm3
    6. Vapor Pressure: 0.000997mmHg at 25°C
    7. Refractive Index: 1.558
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2-(4-BROMOPHENYL)MALONDIALDEHYDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2-(4-BROMOPHENYL)MALONDIALDEHYDE(709648-68-0)
    12. EPA Substance Registry System: 2-(4-BROMOPHENYL)MALONDIALDEHYDE(709648-68-0)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: IRRITANT
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 709648-68-0(Hazardous Substances Data)

709648-68-0 Usage

Uses

Used in Organic Synthesis:
2-(4-BROMOPHENYL)MALONDIALDEHYDE is used as a building block for the synthesis of more complex organic molecules, leveraging its unique structure to create a diverse array of compounds for various applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-(4-BROMOPHENYL)MALONDIALDEHYDE is employed as a precursor for the development of pharmaceuticals, potentially contributing to the creation of new drugs and therapeutic agents. Its specific structural features make it a valuable component in the design and synthesis of bioactive molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 709648-68-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,9,6,4 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 709648-68:
(8*7)+(7*0)+(6*9)+(5*6)+(4*4)+(3*8)+(2*6)+(1*8)=200
200 % 10 = 0
So 709648-68-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H7BrO2/c10-9-3-1-7(2-4-9)8(5-11)6-12/h1-6,8H

709648-68-0SDS

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-bromophenyl)propanedial

1.2 Other means of identification

Product number -
Other names -

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:709648-68-0 SDS

709648-68-0Relevant articles and documents

Design, synthesis and biological evaluation of some novel N-arylpyrazole derivatives bearing the sulfonamide moiety as cytotoxic agents

Duan, Xiaobo,Wang, Yingxing,Feng, Weipei,Yang, Yaxing,Li, Hongyan,Li, Shenghui,Yang, Xiaobing,Zhang, Jinchao,Wang, Shuxiang,Zhou, Guoqiang,Zhou, Chuanqi

, p. 271 - 281 (2017/01/14)

A series of novel N-arylpyrazole derivatives (4a–4l) bearing the sulfonamide moiety were synthesized by the condensation reaction of 1,3-dicarbonyl compounds with 4-hydrazinylbenzenesulfonamide. The structures of the obtained compounds were established on

Synthesis, anticancer activity and DNA-binding properties of novel 4-pyrazolyl-1,8-naphthalimide derivatives

Li, Shenghui,Xu, Shengjie,Tang, Yonghe,Ding, Shan,Zhang, Jinchao,Wang, Shuxiang,Zhou, Guoqiang,Zhou, Chuanqi,Li, Xiaoliu

supporting information, p. 586 - 590 (2014/01/23)

A novel series of 4-pyrazolyl-1,8-naphthalimide derivatives have been designed and facilely synthesized. For anticancer activity in vitro, most of the compounds were found to be more toxic against human mammary cancer cells (MCF-7) than human cervical car

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