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100553-56-8

3-{[(2Z)-2-(nitromethylidene)imidazolidin-1-yl]methyl}pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 100553-56-8 Structure

  • Basic information

    1. Product Name: 3-{[(2Z)-2-(nitromethylidene)imidazolidin-1-yl]methyl}pyridine
    2. Synonyms:
    3. CAS NO:100553-56-8
    4. Molecular Formula: C10H12N4O2
    5. Molecular Weight: 220.2279
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 100553-56-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 408.3°C at 760 mmHg
    3. Flash Point: 200.8°C
    4. Appearance: N/A
    5. Density: 1.369g/cm3
    6. Vapor Pressure: 7.06E-07mmHg at 25°C
    7. Refractive Index: 1.672
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-{[(2Z)-2-(nitromethylidene)imidazolidin-1-yl]methyl}pyridine(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-{[(2Z)-2-(nitromethylidene)imidazolidin-1-yl]methyl}pyridine(100553-56-8)
    12. EPA Substance Registry System: 3-{[(2Z)-2-(nitromethylidene)imidazolidin-1-yl]methyl}pyridine(100553-56-8)

  • 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: 100553-56-8(Hazardous Substances Data)

100553-56-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100553-56-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,5 and 3 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 100553-56:
(8*1)+(7*0)+(6*0)+(5*5)+(4*5)+(3*3)+(2*5)+(1*6)=78
78 % 10 = 8
So 100553-56-8 is a valid CAS Registry Number.

100553-56-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[[(2Z)-2-(nitromethylidene)imidazolidin-1-yl]methyl]pyridine

1.2 Other means of identification

Product number -
Other names 1-(nicotinyl)-2-nitromethyleneimidazolidine

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:100553-56-8 SDS

100553-56-8Relevant articles and documents

Design, synthesis, and bioactivity of cyanonitrovinyl neonicotinoids as potential insecticides

Wang, Kewei,Qian, Xuhong,Cui, Jingnan

, p. 1117 - 1122 (2012/06/18)

A series of cyanonitrovinyl neonicotinoids were designed and synthesized via five steps in about 35% overall yields. All compounds were structurally characterized by 1H nuclear magnetic resonance (NMR), 13C NMR, infrared (IR), and high-resolution mass spectrometry (HRMS), and single-crystal X-ray diffraction analysis of 2-[1-[(6-chloropyridin-3-yl)methyl] -2-imidazolidinylidene]-2-nitroacetonitrile revealed that the double bond is (E)-configured. The preliminary agriculture bioassay indicated that one compound exhibited moderate insecticidal activity against pea aphid. Springer-Verlag 2010.

One step from nitro to oxime: a convenient preparation of unsaturated oximes by the reduction of the corresponding vinylnitro compounds

Wang, Kewei,Qian, Xuhong,Cui, Jingnan

experimental part, p. 10377 - 10382 (2010/02/27)

A series of novel unsaturated oximes were conveniently prepared from the corresponding vinylnitro compounds by reduction with SnCl2·2H2O. The structures of the oximes were characterized by 1H and 13C NMR, IR and HRMS, and X-ray crystallography analysis of 1-(6-chloro-pyridin-3-ylmethyl)-4,5-dihydro-1H-imidazole-2-carbaldehyde oxime 2a reveals that, the hydroxyl group is arranged in a trans configuration. Some evidences from a brief investigation suggest that these oximes seem to be formed by reduction of the aci form of nitro aliphatic compounds.

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