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106861-17-0

4-methylpyridazine-3-carbonitrile is a heterocyclic chemical compound with the molecular formula C6H5N3. It features a pyridazine ring, which is a six-membered aromatic ring containing four nitrogen atoms, with a methyl group and a nitrile functional group attached at the 3-position. 4-methylpyridazine-3-carbonitrile is known for its versatility in organic synthesis and its utility as a building block in the development of pharmaceuticals and agrochemicals.

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  • 106861-17-0 Structure

  • Basic information

    1. Product Name: 4-methylpyridazine-3-carbonitrile
    2. Synonyms: 4-methylpyridazine-3-carbonitrile
    3. CAS NO:106861-17-0
    4. Molecular Formula: C6H5N3
    5. Molecular Weight: 119
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 106861-17-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: Sealed in dry,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-methylpyridazine-3-carbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-methylpyridazine-3-carbonitrile(106861-17-0)
    11. EPA Substance Registry System: 4-methylpyridazine-3-carbonitrile(106861-17-0)

  • 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: 106861-17-0(Hazardous Substances Data)

106861-17-0 Usage

Uses

Used in Pharmaceutical Industry:
4-methylpyridazine-3-carbonitrile is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows for the creation of a wide range of derivatives with different properties and therapeutic applications. It plays a crucial role in the development of new drugs with improved efficacy and selectivity.
Used in Agrochemical Industry:
In the agrochemical sector, 4-methylpyridazine-3-carbonitrile serves as a valuable building block for the synthesis of pesticides and other crop protection agents. Its incorporation into these compounds can enhance their effectiveness in controlling pests and diseases, thereby contributing to increased crop yields and food security.
Used in Organic Synthesis:
4-methylpyridazine-3-carbonitrile is utilized as a versatile intermediate in organic synthesis. Its chemical structure enables the formation of various derivatives with distinct properties, making it a valuable component in the creation of novel compounds for a range of applications, including materials science, dyes, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 106861-17-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,6 and 1 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106861-17:
(8*1)+(7*0)+(6*6)+(5*8)+(4*6)+(3*1)+(2*1)+(1*7)=120
120 % 10 = 0
So 106861-17-0 is a valid CAS Registry Number.

106861-17-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methylpyridazine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 4-METHYL-3-PYRIDAZINECARBONITRILE

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:106861-17-0 SDS

106861-17-0Downstream Products

106861-17-0Relevant articles and documents

Efficient synthesis of 5-substituted-3-pyridazine carbonitrile via regioselective Reissert-type reaction

Wang, Shengqiang,Geng, Zhiyue,Guo, Ruiyun,Li, Jingya,Zou, Dapeng,Wu, Yangjie,Wu, Yusheng

supporting information, p. 3067 - 3070 (2016/07/06)

Various 5-substituted-3-pyridazine carbonitrile derivatives were synthesized by regioselective Reissert-type reaction with 4-substituted pyridazine, 4-methylbenzene-1-sulfonyl chloride and trimethylsilyl cyanide. The reaction can be carried out under cond

PYRIDAZINES XXXI.1,2 A FACILE SYNTHESIS OF 3-PYRIDAZINECARBONITRILES VIA 2-(4-TOLUENESULFONYL)-2,3-DIHYDRO-3-PYRIDAZINECARBONITRILES

Dostal, Wolfgang,Heinish, Gottfried

, p. 793 - 797 (2007/10/02)

Pyridazines 1a-c react with trimethylsilyl cyanide/4-toluenesulfonyl chloride to give 2-(4-toluenesulfonyl)-2,3-dihydro-3-pyridazinecarbonitriles (2a-c) in satisfactory yields.Conversion of compounds 2a-c into 3-pyridazinecarbonitriles 3a-c is convenientl

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