Welcome to LookChem.com Sign In|Join Free

CAS

  • or

25938-99-2

3,4-dichloro-N-phenylbenzohydrazonoyl chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25938-99-2 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 25938-99-2 Structure

  • Basic information

    1. Product Name: 3,4-dichloro-N-phenylbenzohydrazonoyl chloride
    2. Synonyms: 3,4-dichloro-N-phenylbenzohydrazonoyl chloride
    3. CAS NO:25938-99-2
    4. Molecular Formula:
    5. Molecular Weight: 299.587
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 25938-99-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,4-dichloro-N-phenylbenzohydrazonoyl chloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,4-dichloro-N-phenylbenzohydrazonoyl chloride(25938-99-2)
    11. EPA Substance Registry System: 3,4-dichloro-N-phenylbenzohydrazonoyl chloride(25938-99-2)

  • 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: 25938-99-2(Hazardous Substances Data)

25938-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25938-99-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,9,3 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25938-99:
(7*2)+(6*5)+(5*9)+(4*3)+(3*8)+(2*9)+(1*9)=152
152 % 10 = 2
So 25938-99-2 is a valid CAS Registry Number.

25938-99-2Relevant articles and documents

[3+2]-cycloaddition of in situ generated nitrile imines and acetylene for assembling of 1,3-disubstituted pyrazoles with quantitative deuterium labeling

Voronin, Vladimir V.,Ledovskaya, Maria S.,Gordeev, Evgeniy G.,Rodygin, Konstantin S.,Ananikov, Valentine P.

, p. 3819 - 3828 (2018/04/14)

A novel synthetic methodology for the preparation of 1,3-disubstituted pyrazoles from in situ generated nitrile imines and acetylene is reported. The reactions are performed in a simple two-chamber reactor. One part of the reactor is loaded with hydrazonoyl chloride precursors of active nitrile imine species and a base. The other part is used to generate acetylene from CaC2 and water. Partitioning of the reactants improves the yields of desired pyrazoles up to 99% and simplifies their isolation to a simple procedure of solvent evaporation. The approach requires no complex equipment and utilizes inexpensive, safe, and easy to handle calcium carbide as a starting material. A model deuterium incorporation is carried out according to the developed methodology, producing a series of novel 4,5-dideuteropyrazoles with excellent deuterium enrichment. Theoretical calculations on reaction mechanism and characterization of possible intermediate structures were performed.

Method of use, composition, and compounds

-

, (2008/06/13)

Certain benzoyl chloride phenylhydrazones have been found to be active against insects and mites. The benzoyl ring and the phenylhydrazone ring can be substituted with a halogen atom, a nitro group, or an alkyl group of from 1 to 6 carbon atoms, inclusive

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 25938-99-2