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1558002-29-1

(E)-2,5-di-(tert-butylimino)-3-p-tolylfuran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1558002-29-1 Structure

  • Basic information

    1. Product Name: (E)-2,5-di-(tert-butylimino)-3-p-tolylfuran
    2. Synonyms: (E)-2,5-di-(tert-butylimino)-3-p-tolylfuran
    3. CAS NO:1558002-29-1
    4. Molecular Formula:
    5. Molecular Weight: 298.428
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1558002-29-1.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: (E)-2,5-di-(tert-butylimino)-3-p-tolylfuran(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-2,5-di-(tert-butylimino)-3-p-tolylfuran(1558002-29-1)
    11. EPA Substance Registry System: (E)-2,5-di-(tert-butylimino)-3-p-tolylfuran(1558002-29-1)

  • 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: 1558002-29-1(Hazardous Substances Data)

1558002-29-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1558002-29-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,5,8,0,0 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1558002-29:
(9*1)+(8*5)+(7*5)+(6*8)+(5*0)+(4*0)+(3*2)+(2*2)+(1*9)=151
151 % 10 = 1
So 1558002-29-1 is a valid CAS Registry Number.

1558002-29-1Downstream Products

1558002-29-1Relevant articles and documents

An efficient synthesis of 2,5-diimino-furans via Pd-catalyzed cyclization of bromoacrylamides and isocyanides

Jiang, Huanfeng,Yin, Meizhou,Li, Yibiao,Liu, Bifu,Zhao, Jinwu,Wu, Wanqing

, p. 2037 - 2039 (2014)

A novel palladium-catalyzed cyclization of bromoacrylamides with isocyanides gives substituted 2,5-diimino-furans, which can be used as the precursor of maleamides. This reaction presumably proceeds through the oxygen atom of the amide moiety of the bromoacrylamides coordinated to the Pd(ii) centre as a key step.

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