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CAS

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55690-09-0

(E)-4-phenyl-2-(pyrid-2-yl)-3-buten-2-yl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 55690-09-0 Structure

  • Basic information

    1. Product Name: (E)-4-phenyl-2-(pyrid-2-yl)-3-buten-2-yl
    2. Synonyms: (E)-4-phenyl-2-(pyrid-2-yl)-3-buten-2-yl
    3. CAS NO:55690-09-0
    4. Molecular Formula:
    5. Molecular Weight: 225.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 55690-09-0.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: (E)-4-phenyl-2-(pyrid-2-yl)-3-buten-2-yl(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-4-phenyl-2-(pyrid-2-yl)-3-buten-2-yl(55690-09-0)
    11. EPA Substance Registry System: (E)-4-phenyl-2-(pyrid-2-yl)-3-buten-2-yl(55690-09-0)

  • 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: 55690-09-0(Hazardous Substances Data)

55690-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55690-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,6,9 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 55690-09:
(7*5)+(6*5)+(5*6)+(4*9)+(3*0)+(2*0)+(1*9)=140
140 % 10 = 0
So 55690-09-0 is a valid CAS Registry Number.

55690-09-0Downstream Products

55690-09-0Relevant articles and documents

Naphthalene-catalysed lithiation of chlorinated nitrogenated aromatic heterocycles and reaction with electrophiles

Gómez, Inmaculada,Alonso, Emma,Ramón, Diego J.,Yus, Miguel

, p. 4043 - 4052 (2000)

Naphthalene catalysed reductive lithiation of various chloroazines (1, 7, 10, 13) in the presence of different electrophiles yields, after hydrolysis, the expected functionalised heterocycles with one (2, 8), two (11, 14a-d) and three nitrogen atoms in the ring (14e,f). This methodology allowed us to trap in situ the lithium imine derived from the reaction of 2- pyridyllithium with benzonitrile, by reaction with a Grignard reagent in the presence of titanium alkoxides. 2,4-Dimethoxypyrimidines (14a,c,d) are demethylated under acidic conditions to give the corresponding uracil derivatives 16. (C) 2000 Elsevier Science Ltd.

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