Welcome to LookChem.com Sign In|Join Free

CAS

  • or

1443442-42-9

8-tert-butyl-6-(4-chlorophenyl)-5-methylindolizine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1443442-42-9 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 1443442-42-9 Structure

  • Basic information

    1. Product Name: 8-tert-butyl-6-(4-chlorophenyl)-5-methylindolizine
    2. Synonyms: 8-tert-butyl-6-(4-chlorophenyl)-5-methylindolizine
    3. CAS NO:1443442-42-9
    4. Molecular Formula:
    5. Molecular Weight: 297.827
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1443442-42-9.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: 8-tert-butyl-6-(4-chlorophenyl)-5-methylindolizine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8-tert-butyl-6-(4-chlorophenyl)-5-methylindolizine(1443442-42-9)
    11. EPA Substance Registry System: 8-tert-butyl-6-(4-chlorophenyl)-5-methylindolizine(1443442-42-9)

  • 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: 1443442-42-9(Hazardous Substances Data)

1443442-42-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1443442-42-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,3,4,4 and 2 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1443442-42:
(9*1)+(8*4)+(7*4)+(6*3)+(5*4)+(4*4)+(3*2)+(2*4)+(1*2)=139
139 % 10 = 9
So 1443442-42-9 is a valid CAS Registry Number.

1443442-42-9Downstream Products

1443442-42-9Relevant articles and documents

One-pot synthesis of polysubstituted indolizines by an addition/ cycloaromatization sequence

Kucukdisli, Murat,Opatz, Till

, p. 6670 - 6676 (2013/07/26)

Indolizines carrying various substituents in positions 5-8 were obtained from readily available 2-(1H-pyrrol-1-yl)nitriles and α,β-unsaturated ketones or aldehydes in a one-pot procedure. Michael addition of the deprotonated aminonitriles to the acceptors followed by acid-catalyzed electrophilic cyclization produces 5,6-dihydroindolizine-5-carbonitriles. From these stable intermediates, substituted indolizines were obtained via base-induced dehydrocyanation.

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 1443442-42-9