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2,6-dimethylphenyl 4-methylphenyl sulfone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 95127-08-5 Structure
  • Basic information

    1. Product Name: 2,6-dimethylphenyl 4-methylphenyl sulfone
    2. Synonyms: 2,6-dimethylphenyl 4-methylphenyl sulfone
    3. CAS NO:95127-08-5
    4. Molecular Formula:
    5. Molecular Weight: 260.357
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 95127-08-5.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: 2,6-dimethylphenyl 4-methylphenyl sulfone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,6-dimethylphenyl 4-methylphenyl sulfone(95127-08-5)
    11. EPA Substance Registry System: 2,6-dimethylphenyl 4-methylphenyl sulfone(95127-08-5)
  • 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: 95127-08-5(Hazardous Substances Data)

95127-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95127-08-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,1,2 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 95127-08:
(7*9)+(6*5)+(5*1)+(4*2)+(3*7)+(2*0)+(1*8)=135
135 % 10 = 5
So 95127-08-5 is a valid CAS Registry Number.

95127-08-5Downstream Products

95127-08-5Relevant articles and documents

Cross-coupling of organoboronic acids and sulfinate salts using catalytic copper(II) acetate and 1,10-phenanthroline: synthesis of aryl and alkenylsulfones

Huang, Fang,Batey, Robert A.

, p. 7667 - 7672 (2007)

A mild method for the preparation of aryl and alkenylsulfones from the cross-coupling reaction of organoboronic acids and sodium sulfinate salts is described. Optimized conditions utilize a catalytic amount of copper(II) acetate monohydrate with 1,10-phenanthroline as ligand in the presence of 4 ? molecular sieves. A co-solvent mixture of dichloromethane/DMSO was used, with reactions occurring at 40 °C under an atmosphere of oxygen. Reaction at room temperature also yields sulfone product, but in lower yields. The method tolerates a variety of substituents on the organoboronic acid, including amide, aldehyde, halide and nitro functionalities, as well as ortho-substituents. In general, the reaction is found to be less efficient using arylboronic acids bearing electron-withdrawing substituents, or using aryltrifluoroborate salts.

Three diphenyl sulfones

Jeyakanthan, Jeyaraman,Velmurugan,Vam, K. Panneersel,Soriano-Garcia, Manuel,Perumal,Chandrasekaran

, p. 630 - 633 (2007/10/03)

In 2,6-dimethylphenyl 4-nitrophenyl sulfone, C14H13-NO4S, (I), 2,6-dimethylphenyl 4-methylphenyl sulfone, C15H16O2S, (II), and 2-methylphenyl phenyl sulfone, C13H12Os

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