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2-(3-CHLORO-4-FLUOROPHENYL)PYRIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 904325-79-7 Structure
  • Basic information

    1. Product Name: 2-(3-CHLORO-4-FLUOROPHENYL)PYRIDINE
    2. Synonyms: 2-(3-CHLORO-4-FLUOROPHENYL)PYRIDINE
    3. CAS NO:904325-79-7
    4. Molecular Formula: C11H7ClFN
    5. Molecular Weight: 207.63
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 904325-79-7.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: 2-(3-CHLORO-4-FLUOROPHENYL)PYRIDINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(3-CHLORO-4-FLUOROPHENYL)PYRIDINE(904325-79-7)
    11. EPA Substance Registry System: 2-(3-CHLORO-4-FLUOROPHENYL)PYRIDINE(904325-79-7)
  • 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: 904325-79-7(Hazardous Substances Data)

904325-79-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 904325-79-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,4,3,2 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 904325-79:
(8*9)+(7*0)+(6*4)+(5*3)+(4*2)+(3*5)+(2*7)+(1*9)=157
157 % 10 = 7
So 904325-79-7 is a valid CAS Registry Number.

904325-79-7Downstream Products

904325-79-7Relevant articles and documents

The iridium complex compound, an organic electroluminescent device, display device and illuminating device

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Paragraph 0190; 0194-0195, (2020/10/21)

PROBLEM TO BE SOLVED: To provide an iridium complex compound for emitting phosphorescence with a good quantum yield, an organic electroluminescent element which is prepared using the compound and has a long driving life and excellent electrical durability, and a display device and an illumination device using the organic electroluminescent element.SOLUTION: There is provided an iridium complex compound represented by following formula (1). An iridium complex compound having a fluorine atom and a specific substituent efficiently emits phosphorescence. An element prepared using the iridium complex compound has a long driving life and enhanced electrical durability.

Ligand-promoted ruthenium-catalyzed: Meta C-H chlorination of arenes using N -chloro-2,10-camphorsultam

Fan, Zhoulong,Lu, Heng,Cheng, Zhen,Zhang, Ao

supporting information, p. 6008 - 6011 (2018/06/18)

A practical meta C-H chlorination protocol is established via a Ru(0)-catalyzed ortho-metalation strategy. The use of N-chloro-2,10-camphorsultam as a new chlorinating agent is crucial for the success of the current reaction and an N-heterocyclic carbene (NHC) ligand could significantly enhance the reactivity of the catalytic transformation. The mechanistic studies reveal that an unusual ortho C-H ruthenation relay process with ortho chlorination of the C-Ru bond is probably involved.

Microwave-assisted Suzuki coupling reactions with an encapsulated palladium catalyst for batch and continuous-flow transformations

Baxendale, Ian R.,Griffiths-Jones, Charlotte M.,Ley, Steven V.,Tranmer, Geoffrey K.

, p. 4407 - 4416 (2008/02/07)

This article describes the design, optimisation and development of a Suzuki cross-coupling protocol mediated by an efficient palladium-en-capsulated catalyst (Pd EnCat) under microwave irradiation. The methodology has been used in both batch mode for classical library preparation and in continuous-flow applications furnishing multigram quantities of material. Described is a method that uses direct focused microwave heating whilst applying an external cooling source. This enables a lower than normal bulk temperature to be maintained throughout the reaction period leading to significant improvements in the overall yield and purity of the reaction products. Additional aspects of this novel heating protocol are discussed in relation to the prolonged lifetime and enhanced reactivity of the immobilised catalyst system.

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