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92853-85-5

2-chloro-4-phenyl-6-(p-tolyl)-1,3,5-triazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92853-85-5 Structure

  • Basic information

    1. Product Name: 2-chloro-4-phenyl-6-(p-tolyl)-1,3,5-triazine
    2. Synonyms: 2-chloro-4-phenyl-6-(p-tolyl)-1,3,5-triazine
    3. CAS NO:92853-85-5
    4. Molecular Formula:
    5. Molecular Weight: 281.744
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92853-85-5.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: 2-chloro-4-phenyl-6-(p-tolyl)-1,3,5-triazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-chloro-4-phenyl-6-(p-tolyl)-1,3,5-triazine(92853-85-5)
    11. EPA Substance Registry System: 2-chloro-4-phenyl-6-(p-tolyl)-1,3,5-triazine(92853-85-5)

  • 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: 92853-85-5(Hazardous Substances Data)

92853-85-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92853-85-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,8,5 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 92853-85:
(7*9)+(6*2)+(5*8)+(4*5)+(3*3)+(2*8)+(1*5)=165
165 % 10 = 5
So 92853-85-5 is a valid CAS Registry Number.

92853-85-5Downstream Products

92853-85-5Relevant articles and documents

A Sequential Suzuki Coupling Approach to Unsymmetrical Aryl s-Triazines from Cyanuric Chloride

Wang, Chen,Zhang, Jiehui,Tang, Jie,Zou, Gang

, p. 2514 - 2519 (2017)

A practical approach has been developed for efficient synthesis of unsymmetrical aryl s-triazines via highly selective sequential Suzuki coupling of cyanuric chloride (2,4,6-trichlorotriazine) with aryl or vinyl boronic or diarylborinic acids catalysed by 0.1–0.5 mol% Pd(PPh3)2Cl2 under mild conditions. The second and third Suzuki couplings for unsymmetrically trisubstituted aryl s-triazines could be more practically conducted in one-pot procedure. An electron-withdrawing conjugate group at phenyl ring of arylboronic acids was unexpectedly found to completely block the coupling while steric hindrance from an ortho electron-donating substituent could be overcome. (Figure presented.).

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