Welcome to LookChem.com Sign In|Join Free

CAS

  • or
Pyridine-2-carboximidohydrazide, also known as isonicotinic acid hydrazide, is a chemical compound with the molecular formula C6H8N4O. It is a hydrazide derivative of isonicotinic acid and is commonly used as a building block in organic synthesis. This versatile compound possesses a wide range of potential applications across various industries due to its unique chemical properties.

1005-02-3 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1005-02-3 Structure
  • Basic information

    1. Product Name: pyridine-2-carboximidohydrazide
    2. Synonyms: Picolinamide hydrazone;Pyridine-2-carbohydrazide imide;Pyridine-2-carboxamidehydrazone;Pyridine-2-carboxamidrazone;2-PyridinecarboxiMidic acid, hydrazide;PicoliniMidohydrazide;pyridine-2-carboximidohydrazide;2-Pyridinecarbohydrazide imide
    3. CAS NO:1005-02-3
    4. Molecular Formula: C6H8N4
    5. Molecular Weight: 136.15452
    6. EINECS: 213-731-7
    7. Product Categories: N/A
    8. Mol File: 1005-02-3.mol
  • Chemical Properties

    1. Melting Point: 95-96 °C
    2. Boiling Point: 328.4°C at 760 mmHg
    3. Flash Point: 152.4°C
    4. Appearance: /
    5. Density: 1.31g/cm3
    6. Vapor Pressure: 0.00019mmHg at 25°C
    7. Refractive Index: 1.646
    8. Storage Temp.: Sealed in dry,Store in freezer, under -20°C
    9. Solubility: N/A
    10. PKA: 7.38±0.50(Predicted)
    11. CAS DataBase Reference: pyridine-2-carboximidohydrazide(CAS DataBase Reference)
    12. NIST Chemistry Reference: pyridine-2-carboximidohydrazide(1005-02-3)
    13. EPA Substance Registry System: pyridine-2-carboximidohydrazide(1005-02-3)
  • 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: 1005-02-3(Hazardous Substances Data)

1005-02-3 Usage

Uses

Used in Pharmaceutical Industry:
Pyridine-2-carboximidohydrazide is used as a reactant in the production of pharmaceuticals for its ability to serve as a key building block in the synthesis of various drug molecules. Its role in creating new compounds with potential therapeutic effects makes it valuable in drug discovery and development.
Used in Agrochemical Industry:
In the agrochemical sector, pyridine-2-carboximidohydrazide is utilized as a reactant in the synthesis of agrochemicals, contributing to the development of pesticides and other agricultural chemicals that are essential for crop protection and yield enhancement.
Used in Dye Industry:
Pyridine-2-carboximidohydrazide is employed in the dye industry as a reactant for the production of dyes, taking advantage of its chemical structure to create a variety of colored compounds used in various applications, including textiles and printing inks.
Used in Antimicrobial Applications:
Pyridine-2-carboximidohydrazide has been studied for its potential as an anti-tuberculosis agent and has demonstrated promising antimicrobial activity against various bacterial and fungal strains. This makes it a candidate for further research and development in the creation of new antimicrobial agents to combat drug-resistant infections.
Used in Corrosion Inhibition:
Research has explored the use of pyridine-2-carboximidohydrazide in the development of corrosion inhibitors, capitalizing on its chemical properties to protect metals from corrosion, which is crucial in various industrial applications to extend the lifespan of metal structures and equipment.
Used in Analytical Chemistry:
Pyridine-2-carboximidohydrazide also serves as a reagent in analytical chemistry, where it aids in the identification, detection, and quantification of various chemical compounds, contributing to the accuracy and efficiency of analytical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 1005-02-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1005-02:
(6*1)+(5*0)+(4*0)+(3*5)+(2*0)+(1*2)=23
23 % 10 = 3
So 1005-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N4/c7-6(10-8)5-3-1-2-4-9-5/h1-4H,8H2,(H2,7,10)

1005-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Pyridinecarbohydrazonamide

1.2 Other means of identification

Product number -
Other names Pyridine-2-carboxamidrazone

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:1005-02-3 SDS

1005-02-3Relevant articles and documents

A Novel Ratiometric Oxygen Sensor Based On a Sextuple Hydrogen-Bonding Self-Assembly Molecular Heterodimer

Zeng, Hui,Zhang, Cheng,Huang, Yan,Lu, Zhiyun

, p. 873 - 877 (2016)

A novel sextuple hydrogen-bonding (HB) self-assembly molecular heterodimer bearing an iridium complex as the indicator dye and two carbazoles as the reference dye, namely 6HB-Irbt-Cz, was synthesized, and its molecular structure was confirmed by1H NMR,13CNMR, TOF-MS and 2D NMR. Because of the inefficient energy transfer process between the carbazole and iridium complex units, 6HB-Irbt-Cz exhibits distinct ?uorescence/phosphorescence dual emission in neat film state. More importantly, the neat film sample of 6HB-Irbt-Cz could display linear ratiometric optical response toward oxygen in the full oxygen concentration range from 0 to 100 vol%, together with good stability, reversibility and rapid response-recovery times. Note that this represents the first discovery of neat-film-based oxygen sensor capable of showing strictly linear ratiometric Stern-Volmer behavior in the oxygen concentration of 0–100 vol%.

Synthesis and Properties of Main-Chain Phosphorescent Polymer with Iridium Complex

Chen, L.,Li, D.,Lin, M.,Ling, Q.,Liu, Ch.,Xing, G.

, p. 2504 - 2511 (2019)

The main-chain phosphorescent polymers, PFCzIr(PhStz) and PFOIr(PhStz) with iridium complex (4-BrPhBt)2Ir(Pytz), are synthesized by the Suzuki polycondensation, in which the fluorene-carbazole and fluorene segments are used as a polymer backbon

Synthesis of isobornylphenol-containing 3-aryl-1,2,4-triazin-5(4H)-ones

Egorov,Chupakhin,Berezin,Rusinov,Rusinov,Buravlev,Chukicheva,Kuchinc

, p. 914 - 918 (2011)

A method for modification of 3-aryl-1,2,4-triazin-5(4H)-ones with isobornylphenols was proposed. The influence of various acylating agents on the reaction pathway was studied.

Synthesis, crystal structure, bovine serum albumin binding studies of 1,2,4-triazine based copper(I) complexes

Pathaw, Larica,Khamrang, Themmila,Kathiravan, Arunkumar,Velusamy, Marappan

, (2020)

A series of new copper complexes have been synthesized and completely characterized by pivotal analytical techniques. The coordination geometry around copper(I) complex was best described as distorted tetrahedral geometry. The binding of bovine serum albumin with Cu(I) complexes are also been investigated. The Stern–Volmer analysis on quenching data exhibits the presence of the static quenching mechanism. The binding constants were calculated using modified Stern-Volmer, Lineweaver–Burk and Scatchard plots. All the complexes exhibit the binding constants in the order of 104. Thus, these results can contribute to the development of Cu(I) based drugs.

Useful preparation of 6-phenyl-2,2′-bipyridine ligands bearing di-n-butylaminophenyl or gallate derivatives substituted in the 3- or 4-positions

Diring, Stéphane,Retailleau, Pascal,Ziessel, Raymond

, p. 3027 - 3031 (2007)

A simple protocol for the efficient preparation of substituted 6-phenyl-2,2′-bipyridine derivatives is described. A reverse type of Diels-Alder reaction between a 6-phenyl-2-pyridyl-1,3,4-triazine and 4-N,N-di-n-butylaminophenyl- or gallate-ethynyl derivatives at high temperature provide a mixture of two products easily separable by column chromatography. A variety of ligands suitable for the synthesis of cyclometalated platinum complexes have been produced. Additional substitution of the Pt-Cl by various donor-acceptor ethynyl fragments is feasible by mean of copper(I) catalysis. Georg Thieme Verlag Stuttgart.

The blue phosphorescent iridium complexes containing new triazole ligands for OLEDs

Ahn, So Youn,Ha, Yunkyoung

, p. 59 - 66 (2009)

For the application to organic light-emitting diodes (OLEDs), the blue light emitting iridium complexes containing a new triazole (trzl) ancillary ligand were prepared and their photophysical properties was studied with respect to substituent effect at th

A Modular Class of Fluorescent Difluoroboranes: Synthesis, Structure, Optical Properties, Theoretical Calculations and Applications for Biological Imaging

Bachollet, Sylvestre P. J. T.,Volz, Daniel,Fiser, Béla,Münch, Stephan,R?nicke, Franziska,Carrillo, Jokin,Adams, Harry,Schepers, Ute,Gómez-Bengoa, Enrique,Br?se, Stefan,Harrity, Joseph P. A.

, p. 12430 - 12438 (2016)

Ten borylated bipyridines (BOBIPYs) have been synthesized and selected structural modifications have been made that allow useful structure–optical property relationships to be gathered. These systems have been further investigated using DFT calculations and spectroscopic measurements, showing blue to green fluorescence with quantum yields up to 41 %. They allow full mapping of the structure to determine where selected functionalities can be implemented, to tune the optical properties or to incorporate linking groups. The best derivative was thus functionalised with an alkyne linker, which would enable further applications through click chemistry and in this optic, the stability of the fluorophores has been evaluated.

1,2,4-Triazole derivatives as host materials for blue and green phosphorescent organic light-emitting devices

Xu, Huixia,Sun, Peng,Wang, Kexiang,Miao, Yanqin,Yang, Tingting,Wang, Hua,Xu, Bingshe,Wong, Wai-Yeung

, p. 4408 - 4413 (2016)

A novel host material, namely 9-(6-(3-phenyl-5-(pyridin-2-yl)-4H-1,2,4-triazol-4-yl)hexyl)-9H-carbazole (PPHCZ) was designed and synthesized by incorporating 1, 2, 4-triazol as the electron-withdrawing moiety and carbazole as electron-donating moiety using hexyl as bridge. The photophysical, electrochemical, thermal properties and performances in phosphorescent organic light-emitting devices (PhOLED) were thoroughly characterized. PPHCZ with a high triplet energy level (3.01?eV) exhibited an obvious intermolecular interaction in thin film. Green and blue PhOLEDs using fac-tris(2-phenylpyridine)iridium and iridium(III) bis(4,6-difluorophenyl)-pyridinato [Formula presented],C2′]picolinate as phosphorescent dopants have been fabricated.

Luminescence comparison of iridium(III) complexes containing symmetric vs. asymmetric quinolinate ligands

Park, Hye Rim,Ha, Yunkyoung

, p. 67 - 74 (2011)

We have focused our research on development of the iridium complexes, especially with respect to blue and red emission for OLED. Previously, we prepared bis-[2,3-bis(4-fluorophenyl)quinoxalinato]iridium(acetylacetonate) [Ir(2,3-dpqx-F2)2/

Synthesis, structural, DFT calculations and biological studies of rhodium and iridium complexes containing azine Schiff-base ligands

Adhikari, Sanjay,Sutradhar, Dipankar,Shepherd, Samantha L.,Phillips, Roger M.,Chandra, Asit K.,Rao, K. Mohan

, p. 404 - 414 (2016)

The reaction of [Cp*MCl2]2(M?=?Rh/Ir) with N–N′ azine Schiff-base ligands (L1–L4) leads to the formation of mononuclear cationic half-sandwich complexes having the general formula [Cp*M(L)Cl]+(1–8), (M?=?Rh/Ir and L?=?(2-hydroxy-4-methoxybenzylidene)2-pyridylamidrazone (L1), (2-hydroxybenzylidene)2-pyridylamidrazone (L2), (1-(2-hydroxyphenyl)ethylidene)2-pyridylamidrazone (L3) and (1-phenylethylidene)2-pyridylamidrazone (L4). All these complexes were isolated as their hexafluorophosphate salts and fully characterized by spectroscopic and analytical techniques. The molecular structure of complexes (1), (3), (4), (7) and (8) have been determined by single crystal X-ray crystallographic studies which displayed the coordination of the ligand to the metal in a bidentate N∩N fashion through nitrogen atom of pyridine and one azine nitrogen. The chemo-sensitivity activities of the complexes were evaluated against HT-29 (human colorectal cancer) cell line and non-cancer cell line ARPE-19 (human retinal epithelial cells) which revealed that the complexes are moderately cytotoxic to cancer cells over human cells although complex 5 was the most potent among all the compounds. Theoretical studies carried out using DFT and TD-DFT at B3LYP level shows good agreement with the experimental results.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 1005-02-3