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2-(6-chloropyridin-3-yl)acetohydrazide is a chemical compound with the molecular formula C7H9ClN3O. It is a hydrazide derivative featuring a pyridine ring and a chloro substituent. 2-(6-chloropyridin-3-yl)acetohydrazide is recognized for its role as a versatile building block in organic synthesis and pharmaceutical research, enabling the creation of various biologically active compounds with potential medicinal properties.

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  • 846548-86-5 Structure
  • Basic information

    1. Product Name: 2-(6-chloropyridin-3-yl)acetohydrazide
    2. Synonyms: 2-(6-chloropyridin-3-yl)acetohydrazide
    3. CAS NO:846548-86-5
    4. Molecular Formula: C7H8ClN3O
    5. Molecular Weight: 185.61092
    6. EINECS: -0
    7. Product Categories: N/A
    8. Mol File: 846548-86-5.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.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(6-chloropyridin-3-yl)acetohydrazide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(6-chloropyridin-3-yl)acetohydrazide(846548-86-5)
    11. EPA Substance Registry System: 2-(6-chloropyridin-3-yl)acetohydrazide(846548-86-5)
  • 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: 846548-86-5(Hazardous Substances Data)

846548-86-5 Usage

Uses

Used in Organic Synthesis:
2-(6-chloropyridin-3-yl)acetohydrazide is used as a key intermediate for the synthesis of a variety of chemical compounds. Its reactivity allows it to participate in numerous chemical reactions, facilitating the formation of new molecules with potential applications across different industries.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(6-chloropyridin-3-yl)acetohydrazide is utilized as a precursor in the development of drugs. Its ability to form new compounds with biological activity makes it a valuable asset in medicinal chemistry, particularly for the design and synthesis of novel therapeutic agents.
Used in Metal Ion Coordination Chemistry:
2-(6-chloropyridin-3-yl)acetohydrazide has been studied for its potential as a chelating agent. This application is significant in metal ion coordination chemistry, where it can bind to metal ions to form stable complexes, which can be useful in various analytical and industrial processes.
Overall, 2-(6-chloropyridin-3-yl)acetohydrazide is a multifaceted chemical with a broad spectrum of uses in chemistry and pharmacology, underpinning its importance in the development of new materials and medicines.

Check Digit Verification of cas no

The CAS Registry Mumber 846548-86-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,6,5,4 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 846548-86:
(8*8)+(7*4)+(6*6)+(5*5)+(4*4)+(3*8)+(2*8)+(1*6)=215
215 % 10 = 5
So 846548-86-5 is a valid CAS Registry Number.

846548-86-5Relevant articles and documents

Synthesis and insecticidal activity of some 1,3,4-oxadiazoles derived from 2-chloropyridine-5-acetic acid

Holla, B. Shivarama,Prasanna,Poojary, Boja,Rao,Shridhara,Bhat, U. Ganesha

, p. 864 - 868 (2007/10/03)

The synthesis of a number of 1,3,4-oxadiazoles 6a-e is described. 2-Chloropyridine-5-acetic acid 3 is prepared starting from easily available 2-chloro-5-chloromethylpyridine 1, via 2-chloro-5-cyanomethylpyridine 2. Esterification of 3 with methanol in the

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