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1286261-80-0

4′-(methylthio)-N-phenylbiphenyl-2-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1286261-80-0 Structure

  • Basic information

    1. Product Name: 4′-(methylthio)-N-phenylbiphenyl-2-carboxamide
    2. Synonyms: 4′-(methylthio)-N-phenylbiphenyl-2-carboxamide
    3. CAS NO:1286261-80-0
    4. Molecular Formula:
    5. Molecular Weight: 319.427
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1286261-80-0.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: 4′-(methylthio)-N-phenylbiphenyl-2-carboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4′-(methylthio)-N-phenylbiphenyl-2-carboxamide(1286261-80-0)
    11. EPA Substance Registry System: 4′-(methylthio)-N-phenylbiphenyl-2-carboxamide(1286261-80-0)

  • 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: 1286261-80-0(Hazardous Substances Data)

1286261-80-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1286261-80-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,6,2,6 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1286261-80:
(9*1)+(8*2)+(7*8)+(6*6)+(5*2)+(4*6)+(3*1)+(2*8)+(1*0)=170
170 % 10 = 0
So 1286261-80-0 is a valid CAS Registry Number.

1286261-80-0Downstream Products

1286261-80-0Relevant articles and documents

Nickel-Mediated Cross-Coupling of Boronic Acids and Phthalimides for the Synthesis of Ortho-Substituted Benzamides

Ahlgrim, Grace C.,Deglopper, Kimberly S.,Dennis, Joseph M.,Heyboer, Ethan M.,Johnson, Jeffrey B.,Johnson, Rebecca L.,Kwiatkowski, Megan R.,Pankratz, Trey C.,Yoder, Mason C.

, p. 3757 - 3765 (2020)

The decarbonylative coupling of phthalimides with aryl boronic acids provides ready access to a broad range of ortho-substituted benzamides. This nickel-mediated methodology extends reactivity from previously described air-sensitive diorganozinc reagents of limited availability to easily handled and widely commercially available boronic acids. The decarbonylative coupling is tolerant of a broad range of functional groups and demonstrates little sensitivity to steric factors on either of the coupling partners.

Nickel-mediated decarbonylative cross-coupling of phthalimides with in situ generated diorganozinc reagents

Havlik, Sarah E.,Simmons, Jessica M.,Winton, Valerie J.,Johnson, Jeffrey B.

experimental part, p. 3588 - 3593 (2011/06/26)

The nickel-mediated cross-coupling of phthalimides with diorganozinc reagents proceeds via a decarbonylative process to produce ortho-substituted benzamides in high yields. In addition to tolerating diverse phthalimide functionality, including alkyl, aryl

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