Welcome to LookChem.com Sign In|Join Free

CAS

  • or

146470-10-2

C14H12Cl2N4*ClH is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

146470-10-2 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 146470-10-2 Structure

  • Basic information

    1. Product Name: C14H12Cl2N4*ClH
    2. Synonyms:
    3. CAS NO:146470-10-2
    4. Molecular Formula:
    5. Molecular Weight: 343.643
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146470-10-2.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: C14H12Cl2N4*ClH(CAS DataBase Reference)
    10. NIST Chemistry Reference: C14H12Cl2N4*ClH(146470-10-2)
    11. EPA Substance Registry System: C14H12Cl2N4*ClH(146470-10-2)

  • 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: 146470-10-2(Hazardous Substances Data)

146470-10-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146470-10-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,4,7 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 146470-10:
(8*1)+(7*4)+(6*6)+(5*4)+(4*7)+(3*0)+(2*1)+(1*0)=122
122 % 10 = 2
So 146470-10-2 is a valid CAS Registry Number.

146470-10-2Downstream Products

146470-10-2Relevant articles and documents

Antiarrhythmic active amidinohydrazones of substituted benzophenones. Part 1: Synthesis of new amidinohydrazones and N-phenylamidinohydrazones of substituted benzophenones

Richter,Kasbohm,Besch,Hagen

, p. 758 - 764 (2007/10/02)

The title compounds are synthesized as a rule by condensation of substituted benzophenones and derivatives of aminoguanidine in the presence of up to 2,5 moles of an anorganic acid. They can be obtained alternatively via corresponding hydrazones, thiosemicarbazones or methylthiothiocarbonylhydrazones.

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 146470-10-2