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CAS

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107266-91-1

3-(Toluene-4-sulfonylmethyl)-biphenyl-4-ylamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 107266-91-1 Structure

  • Basic information

    1. Product Name: 3-(Toluene-4-sulfonylmethyl)-biphenyl-4-ylamine
    2. Synonyms: 3-(Toluene-4-sulfonylmethyl)-biphenyl-4-ylamine
    3. CAS NO:107266-91-1
    4. Molecular Formula:
    5. Molecular Weight: 337.442
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 107266-91-1.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: 3-(Toluene-4-sulfonylmethyl)-biphenyl-4-ylamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(Toluene-4-sulfonylmethyl)-biphenyl-4-ylamine(107266-91-1)
    11. EPA Substance Registry System: 3-(Toluene-4-sulfonylmethyl)-biphenyl-4-ylamine(107266-91-1)

  • 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: 107266-91-1(Hazardous Substances Data)

107266-91-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 107266-91-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,2,6 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 107266-91:
(8*1)+(7*0)+(6*7)+(5*2)+(4*6)+(3*6)+(2*9)+(1*1)=121
121 % 10 = 1
So 107266-91-1 is a valid CAS Registry Number.

107266-91-1Relevant articles and documents

A Facile Synthesis of 3-Sulfonyl-Substituted Indole Derivatives

Wojciechowski, Krzysztof,Makosza, Mieczyslaw

, p. 651 - 653 (1986)

A new method for the synthesis of 3-sulfonyl-substituted indole derivatives 5 was developed starting from the easily available products of the vicarious nucleophilic substitution of hydrogen in nitroarenes 1.

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