Welcome to LookChem.com Sign In|Join Free

CAS

  • or
N-hydroxy-N'-(1,1-dimethylethyl)-benzenecarboximidamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20002-26-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 20002-26-0 Structure
  • Basic information

    1. Product Name: N-hydroxy-N'-(1,1-dimethylethyl)-benzenecarboximidamide
    2. Synonyms: N-hydroxy-N'-(1,1-dimethylethyl)-benzenecarboximidamide
    3. CAS NO:20002-26-0
    4. Molecular Formula:
    5. Molecular Weight: 192.261
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 20002-26-0.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: N-hydroxy-N'-(1,1-dimethylethyl)-benzenecarboximidamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-hydroxy-N'-(1,1-dimethylethyl)-benzenecarboximidamide(20002-26-0)
    11. EPA Substance Registry System: N-hydroxy-N'-(1,1-dimethylethyl)-benzenecarboximidamide(20002-26-0)
  • 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: 20002-26-0(Hazardous Substances Data)

20002-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20002-26-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,0 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20002-26:
(7*2)+(6*0)+(5*0)+(4*0)+(3*2)+(2*2)+(1*6)=30
30 % 10 = 0
So 20002-26-0 is a valid CAS Registry Number.

20002-26-0Relevant articles and documents

Easy Access to 1-Amino and 1-Carbon Substituted Isoquinolines via Cobalt-Catalyzed C - H/N - O Bond Activation

Muralirajan, Krishnamoorthy,Kuppusamy, Ramajayam,Prakash, Sekar,Cheng, Chien-Hong

supporting information, p. 774 - 783 (2016/03/09)

A green atom-economical method for the synthesis of highly functionalized 1-amino and 1-carbon substituted isoquinolines from the reaction of N′-hydroxybenzimidamides and aryl ketoximes, respectively, with alkynes via pentamethylcyclopentadienylcobalt(III)-catalyzed C - H/N - O bond activation is described. The external oxidant-free annulation reaction uses the =NOH moiety in N′-hydroxybenzimidamides or N-aromatic ketone oximes as the directing group and internal oxidant. This first row transition metal-catalyzed annulation serves as an efficient alternative for the synthesis of isoquinolines, as water is the only by-product and expensive noble metals such as rhodium(III), iridium(III), palladium(II), and ruthenium(II) are not required. The reaction proceeds via C - H activation, alkyne insertion, reductive elimination, and N - O activation.

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 20002-26-0