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3-(4-Bromophenyl)-5-methylisoxazole-4-carboxaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1119449-35-2 Structure
  • Basic information

    1. Product Name: 3-(4-Bromophenyl)-5-methylisoxazole-4-carboxaldehyde
    2. Synonyms: 3-(4-Bromophenyl)-5-methylisoxazole-4-carboxaldehyde;3-(4-bromophenyl)-5-methyl-1,2-oxazole-4-carbaldehyde
    3. CAS NO:1119449-35-2
    4. Molecular Formula: C11H8BrNO2
    5. Molecular Weight: 266.09072
    6. EINECS: N/A
    7. Product Categories: Heterocyclic Building BlocksBuilding Blocks;Chemical Synthesis;Heterocyclic Building Blocks;Isoxazoles;New Products for Chemical Synthesis
    8. Mol File: 1119449-35-2.mol
  • Chemical Properties

    1. Melting Point: 102-107 °C
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-(4-Bromophenyl)-5-methylisoxazole-4-carboxaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-Bromophenyl)-5-methylisoxazole-4-carboxaldehyde(1119449-35-2)
    11. EPA Substance Registry System: 3-(4-Bromophenyl)-5-methylisoxazole-4-carboxaldehyde(1119449-35-2)
  • Safety Data

    1. Hazard Codes: Xn
    2. Statements: 22-36/37/38
    3. Safety Statements: 26
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1119449-35-2(Hazardous Substances Data)

1119449-35-2 Usage

Abbreviation

BMIMC

Physical Appearance

Yellow crystalline solid

Utility

Synthesis: Commonly used as a building block in pharmaceuticals and agrochemicals synthesis.
Functional Groups: Contains a bromo-phenyl group and a methyl-isoxazole group, facilitating the development of biologically active compounds.
Reactivity: Versatile reagent in organic synthesis.
Functionalization: Aldehyde group allows for further functionalization and derivatization.

Applications

Drug Discovery: Useful in creating new chemical entities for potential drug applications.
Biological Activity: Studied for potential anti-inflammatory and anticancer properties.

Industrial Importance

Important intermediate in the production of various organic chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 1119449-35-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,9,4,4 and 9 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1119449-35:
(9*1)+(8*1)+(7*1)+(6*9)+(5*4)+(4*4)+(3*9)+(2*3)+(1*5)=152
152 % 10 = 2
So 1119449-35-2 is a valid CAS Registry Number.

1119449-35-2 Well-known Company Product Price

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  • Aldrich

  • (699934)  3-(4-Bromophenyl)-5-methylisoxazole-4-carboxaldehyde  97%

  • 1119449-35-2

  • 699934-1G

  • 1,263.60CNY

  • Detail

1119449-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-Bromophenyl)-5-methyl-1,2-oxazole-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3-(4-Bromophenyl)-5-methylisoxazole-4-carboxaldehyde

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:1119449-35-2 SDS

1119449-35-2Downstream Products

1119449-35-2Relevant articles and documents

Dimeric isoxazolyl-1,4-dihydropyridines have enhanced binding at the multi-drug resistance transporter

Steiger, Scott A.,Li, Chun,Backos, Donald S.,Reigan, Philip,Natale

, p. 3223 - 3234 (2017)

A series of dimeric isoxazolyl-1,4-dihydropyridines (IDHPs) were prepared by click chemistry and examined for their ability to bind the multi-drug resistance transporter (MDR-1), a member of the ATP-binding cassette superfamily (ABC). Eight compounds in t

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