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CAS

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127257-60-7

1-(2-pyridyl)-3-phenylisobenzofuran is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127257-60-7 Structure

  • Basic information

    1. Product Name: 1-(2-pyridyl)-3-phenylisobenzofuran
    2. Synonyms: 1-(2-pyridyl)-3-phenylisobenzofuran
    3. CAS NO:127257-60-7
    4. Molecular Formula:
    5. Molecular Weight: 271.318
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127257-60-7.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: 1-(2-pyridyl)-3-phenylisobenzofuran(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-pyridyl)-3-phenylisobenzofuran(127257-60-7)
    11. EPA Substance Registry System: 1-(2-pyridyl)-3-phenylisobenzofuran(127257-60-7)

  • 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: 127257-60-7(Hazardous Substances Data)

127257-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127257-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,2,5 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 127257-60:
(8*1)+(7*2)+(6*7)+(5*2)+(4*5)+(3*7)+(2*6)+(1*0)=127
127 % 10 = 7
So 127257-60-7 is a valid CAS Registry Number.

127257-60-7Relevant articles and documents

A One-pot preparation of 1,3-diarylisobenzofuran

Hamura, Toshiyuki,Nakayama, Ryosuke

, p. 1013 - 1015 (2013/09/24)

A simple, practical, and efficient method for one-pot synthesis of symmetric and unsymmetrical 1,3-diarylisobenzofurans has been developed by sequential reactions of methyl 2-formylbenzoate with two identical or different aryl metal species.

Regioselective Synthesis of Substituted Rubrenes

Dodge, Jeffrey A.,Bain, J. D.,Chamberlin, A. Richard

, p. 4190 - 4198 (2007/10/02)

The development of two complementary synthetic routes to 5,6,11,12-tetraphenylnaphthacene (rubrene) derivatives is described.In one approach, selective nucleophilic addition of aryllithiums to diarylnaphthacenequinones (13, 14, 16), followed by HI aromatization of the corresponding diols, allows for the convenient preparation of a wide variety of selectively functionalized rubrenes.Symmetrically and unsymmetrically di- and tetrasubstituted rubrenes have been prepared, as well as several "end-capped" versions.In a second route, cycloaddition of 1,3-diphenylisobenzofuran with the naphthyne 7 (Ar= Ph) followed by Lewis acid mediated deoxygenation of the resultant oxo-bridged adduct gives rubrene in a particularly convergent manner.Elaboration through the use of substituted isobenzofurans (i.e. 9-11) allows for the analogous preparation of substituted rubrenes (45-47).

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