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CAS

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66549-34-6

3-CHLORO-6-(3-METHYLPHENYL)-PYRIDAZINE is a chemical compound with the molecular formula C10H8ClN3. It is a pyridazine derivative featuring a chlorine atom and a 3-methylphenyl group attached to the 3 and 6 positions, respectively. 3-CHLORO-6-(3-METHYLPHENYL)-PYRIDAZINE is known for its unique structure and reactivity, making it a valuable intermediate in the synthesis of various biologically active compounds.

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  • 66549-34-6 Structure

  • Basic information

    1. Product Name: 3-CHLORO-6-(3-METHYLPHENYL)-PYRIDAZINE
    2. Synonyms: 3-CHLORO-6-(3-METHYLPHENYL)-PYRIDAZINE;3-(6-Chloropyridazin-3-yl)toluene, 3-Chloro-6-(3-methylphenyl)-1,2-diazine
    3. CAS NO:66549-34-6
    4. Molecular Formula: C11H9ClN2
    5. Molecular Weight: 204.66
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 66549-34-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 374.596 °C at 760 mmHg
    3. Flash Point: 212.13 °C
    4. Appearance: /
    5. Density: 1.208 g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.585
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-CHLORO-6-(3-METHYLPHENYL)-PYRIDAZINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-CHLORO-6-(3-METHYLPHENYL)-PYRIDAZINE(66549-34-6)
    12. EPA Substance Registry System: 3-CHLORO-6-(3-METHYLPHENYL)-PYRIDAZINE(66549-34-6)

  • Safety Data

    1. Hazard Codes: Xi
    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: 66549-34-6(Hazardous Substances Data)

66549-34-6 Usage

Uses

Used in Pharmaceutical Industry:
3-CHLORO-6-(3-METHYLPHENYL)-PYRIDAZINE is used as a building block for the synthesis of drugs. Its unique structure allows it to be a key component in the development of new pharmaceuticals with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-CHLORO-6-(3-METHYLPHENYL)-PYRIDAZINE serves as a precursor for the production of pesticides. Its reactivity and structural features contribute to the creation of effective pest control agents.
Used in Research and Development:
3-CHLORO-6-(3-METHYLPHENYL)-PYRIDAZINE is also utilized in research and development for the creation of new chemical entities. Its potential applications in this field are vast, as it can be used to explore and develop compounds with novel properties and uses.

Check Digit Verification of cas no

The CAS Registry Mumber 66549-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,5,4 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66549-34:
(7*6)+(6*6)+(5*5)+(4*4)+(3*9)+(2*3)+(1*4)=156
156 % 10 = 6
So 66549-34-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H9ClN2/c1-8-3-2-4-9(7-8)10-5-6-11(12)14-13-10/h2-7H,1H3

66549-34-6SDS

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 3-chloro-6-(3-methylphenyl)pyridazine

1.2 Other means of identification

Product number -
Other names 3-chloro-6-m-tolyl-pyridazine

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:66549-34-6 SDS

66549-34-6Relevant articles and documents

Pd-catalyzed chemoselective cross-coupling reaction of triaryl- or triheteroarylbismuth compounds with 3,6-dihalopyridazines

Urgin, Karene,Aube, Christophe,Pipelier, Muriel,Blot, Virginie,Thobie-Gautier, Christine,Sengmany, Stephane,Lebreton, Jacques,Leonel, Eric,Dubreuil, Didier,Condon, Sylvie

supporting information, p. 117 - 124 (2013/02/22)

The cross-coupling reactions of 3,6-dihalopyridazines with triaryl- or triheteroarylbismuth compounds were performed under palladium catalysis. The reaction was highly chemoselective, affording functionalized aryl- or heteroarylpyridazinyl chlorides in moderate to good yields. The cross-coupling reactions of 3,6-dihalopyridazines with triaryl- or triheteroarylbismuth compounds were performed under palladium catalysis. The reaction was highly chemoselective, affording functionalized aryl- or heteroarylpyridazinyl chlorides in moderate to good yields. Copyright

6-Phenyl-1,2,4-triazolo[4,3-b]pyridazine hypotensive agents

-

, (2008/06/13)

This disclosure describes novel substituted 6-phenyl-1,2,4-triazolo[4,3-b]pyridazines useful as hypotensive agents.

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