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CAS

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73153-48-7

Benzamide, N-[2-(methylsulfonyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 73153-48-7 Structure

  • Basic information

    1. Product Name: Benzamide, N-[2-(methylsulfonyl)phenyl]-
    2. Synonyms:
    3. CAS NO:73153-48-7
    4. Molecular Formula: C14H13NO3S
    5. Molecular Weight: 275.328
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 73153-48-7.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: Benzamide, N-[2-(methylsulfonyl)phenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzamide, N-[2-(methylsulfonyl)phenyl]-(73153-48-7)
    11. EPA Substance Registry System: Benzamide, N-[2-(methylsulfonyl)phenyl]-(73153-48-7)

  • 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: 73153-48-7(Hazardous Substances Data)

73153-48-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73153-48-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,5 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73153-48:
(7*7)+(6*3)+(5*1)+(4*5)+(3*3)+(2*4)+(1*8)=117
117 % 10 = 7
So 73153-48-7 is a valid CAS Registry Number.

73153-48-7Relevant articles and documents

Synthesis of 4H-1,4-Benzothiazines via Lithiation Alpha to Sulphur of 2-Acylaminophenyl Alkyl Sulphides, Sulphoxides, and Sulphones

Babudri, Francesco,Florio, Saverio,Vitrani, Anna Maria,Nunno, Leonardo Di

, p. 1899 - 1903 (2007/10/02)

4H-1,4-Benzothiazines, their monoxides, and their dioxides are readily prepared via lithiation and intramolecular cyclisation of 2-acylaminophenyl alkyl sulphides, sulphoxides, and sulphones with lithium di-isopropylamide in tetrahydrofuran at -50 deg C.

Radical Pair Mechanism in the Aromatic Rearrangement of O-Alkylsulfinyl-N-phenylhydroxylamines

Heesing, Albert,Kleine Homann, Walter,Muellers, Wolfgang

, p. 152 - 164 (2007/10/02)

O-Alkylsulfinyl-N-benzoyl-N-phenylhydroxylamines (3) rearrange at -70 degC to give sulfonamides 4, o-sulfones 5, p-sulfones 6, and o-sulfonates 7.These reactions proceed intramolecularly via the radical pair 13 by -, - and -shifts in both radicals as proved both by experiments with 18O-indicated N-benzoyl-N-phenylhydroxylamine (1) and by strong 13C-CIDNP effects.The third oxygen in the o-sulfonate 7 is donated by a second molecule of the educt 1.

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