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N,N-dimethyl-4-nitrosoanilinium chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 42344-05-8 Structure
  • Basic information

    1. Product Name: N,N-dimethyl-4-nitrosoanilinium chloride
    2. Synonyms: N,N-dimethyl-4-nitrosoanilinium chloride
    3. CAS NO:42344-05-8
    4. Molecular Formula: C8H10N2O*ClH
    5. Molecular Weight: 186.63874
    6. EINECS: 255-762-9
    7. Product Categories: N/A
    8. Mol File: 42344-05-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 258.7°C at 760 mmHg
    3. Flash Point: 110.3°C
    4. Appearance: /
    5. Density: N/A
    6. Vapor Pressure: 0.0135mmHg at 25°C
    7. Refractive Index: N/A
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: N,N-dimethyl-4-nitrosoanilinium chloride(CAS DataBase Reference)
    11. NIST Chemistry Reference: N,N-dimethyl-4-nitrosoanilinium chloride(42344-05-8)
    12. EPA Substance Registry System: N,N-dimethyl-4-nitrosoanilinium chloride(42344-05-8)
  • 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: 42344-05-8(Hazardous Substances Data)

42344-05-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 42344-05-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,3,4 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 42344-05:
(7*4)+(6*2)+(5*3)+(4*4)+(3*4)+(2*0)+(1*5)=88
88 % 10 = 8
So 42344-05-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O.ClH/c1-10(2)8-5-3-7(9-11)4-6-8;/h3-6H,1-2H3;1H

42344-05-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-dimethyl-4-nitroso-Benzenamine, hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:42344-05-8 SDS

42344-05-8Relevant articles and documents

Vaginitis treating compound and use thereof (by machine translation)

-

Paragraph 0030; 0031; 0032, (2016/10/07)

The invention relates to a compound for treating vaginitis and application thereof. The structure of the compound is as shown in the specification, wherein n is any integer from 2 to 6; R1=3-CL, 4-F; 4-CBr3, or 3,4-II-Br; R2 is as shown in the specification. The compound provided by the invention can remarkably inhibit common strains in vaginitis, therefore has significance in clinic practice, and is expected to be developed into a novel medicine for effectively treat vaginitis.

Synthesis and characterization of 2,7-bis(2-pyridyl)-1,8-diazaanthraquinone - A redox-active ligand designed for the construction of supramolecular grids

Jain, Rajsapan,Caldwell, Sharon L.,Louie, Anika S.,Hicks, Robin G.

, p. 1263 - 1267 (2008/01/27)

Double condensation of 2-acetylpyridine with 1,3-diaminobenzene-4,6- dicarboxaldehyde affords 2,7-bis(2-pyridyl)-1,8-diazaanthracene, which was subsequently oxidized to the corresponding quinone. Electrochemical studies indicate two reversible reduction processes corresponding to semiquinone and hydroquinonate formation. Electron-withdrawing pyridine groups and the nitrogen atoms make this somewhat more easily reduced than anthraquinone. This compound is redox-active and can be reduced to its radical anion, a potential spin-bearing ligand for the construction of [2 x 2] metallo-grid structures.

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