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4-[4,5-bis(4-methoxyphenyl)-1H-imidazol-2-yl]benzonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 107701-40-6 Structure
  • Basic information

    1. Product Name: 4-[4,5-bis(4-methoxyphenyl)-1H-imidazol-2-yl]benzonitrile
    2. Synonyms: 4-[4,5-bis(4-methoxyphenyl)-1H-imidazol-2-yl]benzonitrile
    3. CAS NO:107701-40-6
    4. Molecular Formula: C24H19N3O2
    5. Molecular Weight: 381.43
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107701-40-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-[4,5-bis(4-methoxyphenyl)-1H-imidazol-2-yl]benzonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-[4,5-bis(4-methoxyphenyl)-1H-imidazol-2-yl]benzonitrile(107701-40-6)
    11. EPA Substance Registry System: 4-[4,5-bis(4-methoxyphenyl)-1H-imidazol-2-yl]benzonitrile(107701-40-6)
  • 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: 107701-40-6(Hazardous Substances Data)

107701-40-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107701-40-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,7,0 and 1 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 107701-40:
(8*1)+(7*0)+(6*7)+(5*7)+(4*0)+(3*1)+(2*4)+(1*0)=96
96 % 10 = 6
So 107701-40-6 is a valid CAS Registry Number.

107701-40-6Downstream Products

107701-40-6Relevant articles and documents

BORONIC ACID-BASED COMPOUND AND METHOD FOR PREPARATION THEREOF

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Paragraph 0084; 0088; 0125-0130, (2019/01/04)

The present invention relates to a boronic acid-based compound and a preparation method thereof. More specifically, the present invention provides: a derivative containing boronic acid and imidazole obtained by substituting various functional groups during a synthesizing process of a boronic acid-based compound; and a preparation method of the derivative in high yield without using an oxidant.COPYRIGHT KIPO 2018

Novel charge-transfer chromophores featuring imidazole as Π-linkage

Patel, Anjan,Bures, Filip,Ludwig, Miroslav,Kulhanek, Jiri,Pytela, Oldrich,Ruzicka, Ales

experimental part, p. 999 - 1013 (2009/09/30)

Overall 21 imidazole-based chromophores have been synthesized and fully characterized. The imidazole core was systematically substituted with donors (NMe2 and OMe) and acceptors (NO2 and CN groups) additionally separated from the imi

Crystal structures and solution spectroscopy of lophine derivatives

Fridman, Natalya,Kaftory, Menahem,Eichen, Yoav,Speiser, Shammai

experimental part, p. 101 - 109 (2009/04/07)

Lophine (2,4,5-triphenylimidazole) derivatives were synthesized and their physicochemical properties were determined. Spectroscopic and fluorescence behavior of lophine derivatives in methanol at different pH and various solvents were presented. The observed spectroscopic features in the solution are determined by specific interactions of the NH hydrogen. These kinds of interactions are manifested both in the solid state and in solution. The crystal and molecular structures of lophine derivatives with different solvents of crystallization are presented and discussed. In all solvates the solvent molecules link host molecules through hydrogen bonds.

Chromotropism of Imidazole Derivatives. Part 1. 4,5-Bis-(4-methoxyphenyl)-2-(4-nitrophenyl)imidazolium Acetate Dihydrate

Sakaino, Yoshiko,Takizawa, Toshiharu,Inouye, Yoshinobu,Kakisawa, Hiroshi

, p. 1623 - 1630 (2007/10/02)

4,5-Bis(4-methoxyphenyl)-2-(4-nitrophenyl)imidazolium acetate dihydrate (1) in the crystalline state exhibits a sensitive colour change from orange-yellow to red on treatment by various methods (drying, trituration, or heating).The colour change was reversible below 70 deg C but above 70 deg C the change was irreversible and the colour deepended.Compound (1) was deprotonated with the loss of one mole of water of crystallization under treatment and can revert to the original by absorption of one mole of water.On heating to 100 deg C, (1) lost all solvent of crystallization to give a deep red material (2). (2) Was considered to be 4,5-bis-(4-methoxyphenyl)-2-(4-nitrophenyl)imidazole which was linked by hydrogen bond from the imino group in one molecule to the nitro oxygen in another.Compound (2) reverted to (1) in saturated AcOH-H2O vapour.

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