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856702-64-2

2-(2'-pyridino)pyrrole-1-tert-butylcarboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 856702-64-2 Structure

  • Basic information

    1. Product Name: 2-(2'-pyridino)pyrrole-1-tert-butylcarboxylate
    2. Synonyms:
    3. CAS NO:856702-64-2
    4. Molecular Formula:
    5. Molecular Weight: 244.293
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 856702-64-2.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: 2-(2'-pyridino)pyrrole-1-tert-butylcarboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2'-pyridino)pyrrole-1-tert-butylcarboxylate(856702-64-2)
    11. EPA Substance Registry System: 2-(2'-pyridino)pyrrole-1-tert-butylcarboxylate(856702-64-2)

  • 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: 856702-64-2(Hazardous Substances Data)

856702-64-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 856702-64-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,7,0 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 856702-64:
(8*8)+(7*5)+(6*6)+(5*7)+(4*0)+(3*2)+(2*6)+(1*4)=192
192 % 10 = 2
So 856702-64-2 is a valid CAS Registry Number.

856702-64-2Downstream Products

856702-64-2Relevant articles and documents

General suzuki coupling of heteroaryl bromides by using tri-tert-butylphosphine as a supporting ligand

Zou, Yinjun,Yue, Guizhou,Xu, Jianwei,Zhou, Jianrong

, p. 5901 - 5905 (2014)

A general procedure for the fast Suzuki coupling of major families of heteroaryl bromides was realized by using Pd(OAc)2/PtBu3 as the catalyst. Many couplings were finished within minutes at room temperature in n-butanol. Different from previous studies, three typical heteroaryl bromides were systematically examined in couplings of various heteroaryl and aryl boronic acids. A fast, general coupling of heteroaryl bromides is realized by using a single palladium catalyst supported by tri-tert-butylphosphine.

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