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5-BROMO-2-(PYRIDIN-3-YLMETHOXY)BENZALDEHYDE is a chemical compound with the molecular formula C13H10BrNO2. It is a brominated benzaldehyde derivative containing a pyridine moiety and a methoxy group. 5-BROMO-2-(PYRIDIN-3-YLMETHOXY)BENZALDEHYDE is characterized by its unique structural features, which make it a valuable building block in organic synthesis and pharmaceutical research.

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  • 892873-56-2 Structure
  • Basic information

    1. Product Name: 5-BROMO-2-(PYRIDIN-3-YLMETHOXY)BENZALDEHYDE
    2. Synonyms: 5-BROMO-2-(PYRIDIN-3-YLMETHOXY)BENZALDEHYDE;AKOS BBV-005058;ASISCHEM C31414;UKRORGSYN-BB BBV-005058;5-bromo-2-(3-pyridylmethoxy)benzaldehyde
    3. CAS NO:892873-56-2
    4. Molecular Formula: C13H10BrNO2
    5. Molecular Weight: 292.13
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 892873-56-2.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 434.221°C at 760 mmHg
    3. Flash Point: 216.409°C
    4. Appearance: /
    5. Density: 1.496g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.636
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 5-BROMO-2-(PYRIDIN-3-YLMETHOXY)BENZALDEHYDE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 5-BROMO-2-(PYRIDIN-3-YLMETHOXY)BENZALDEHYDE(892873-56-2)
    12. EPA Substance Registry System: 5-BROMO-2-(PYRIDIN-3-YLMETHOXY)BENZALDEHYDE(892873-56-2)
  • 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: 892873-56-2(Hazardous Substances Data)

892873-56-2 Usage

Uses

Used in Pharmaceutical Research:
5-BROMO-2-(PYRIDIN-3-YLMETHOXY)BENZALDEHYDE is used as a building block in the development of new drugs and biologically active molecules. Its structural properties and potential biological activity make it a promising candidate for further investigation in drug discovery and development.
Used in Medicinal Chemistry:
5-BROMO-2-(PYRIDIN-3-YLMETHOXY)BENZALDEHYDE is utilized in medicinal chemistry for its structural features, which allow it to be a versatile reagent in the preparation of various heterocyclic compounds. These heterocyclic compounds are essential in the synthesis of pharmaceuticals and other bioactive molecules.
Used in Organic Synthesis:
In the field of organic synthesis, 5-BROMO-2-(PYRIDIN-3-YLMETHOXY)BENZALDEHYDE serves as a key intermediate for the synthesis of complex organic molecules. Its unique structure allows for a wide range of chemical reactions, making it a valuable component in the creation of novel compounds with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 892873-56-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,2,8,7 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 892873-56:
(8*8)+(7*9)+(6*2)+(5*8)+(4*7)+(3*3)+(2*5)+(1*6)=232
232 % 10 = 2
So 892873-56-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H10BrNO2/c14-12-3-4-13(11(6-12)8-16)17-9-10-2-1-5-15-7-10/h1-8H,9H2

892873-56-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-BROMO-2-(PYRIDIN-3-YLMETHOXY)BENZALDEHYDE

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:892873-56-2 SDS

892873-56-2Downstream Products

892873-56-2Relevant articles and documents

Synthesis and biological evaluation of rhodanine derivatives as PRL-3 inhibitors

Ahn, Jin Hee,Kim, Seung Jun,Park, Woul Seong,Cho, Sung Yun,Ha, Jae Du,Kim, Sung Soo,Kang, Seung Kyu,Jeong, Dae Gwin,Jung, Suk-Kyeong,Lee, Sang-Hyeup,Kim, Hwan Mook,Park, Song Kyu,Lee, Ki Ho,Lee, Chang Woo,Ryu, Seong Eon,Choi, Joong-Kwon

, p. 2996 - 2999 (2008/09/20)

A series of rhodanine derivatives was synthesized and evaluated for their ability to inhibit PRL-3. Benzylidene rhodanine derivative showed good biological activity, while compound 5e was the most active in this series exhibiting an IC50 value of 0.9 μM in vitro and showed a reduced invasion in cell-based assay.

Palladium catalyzed α-arylation of methyl isobutyrate and isobutyronitrile: an efficient synthesis of 2,5-disubstituted benzyl alcohol and amine intermediates

Shetty, Rupa,Moffett, Kristofer K.

, p. 8021 - 8024 (2007/10/03)

Several 2,5-disubstituted benzyl alcohols containing a functionalized t-butyl moiety were synthesized via palladium catalyzed α-arylation of methyl isobutyrate and butyronitrile on synthetically useful scales. The resulting benzyl alcohols could then be further elaborated to benzyl amines or other desirable intermediates.

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