BENZENESULFONYL ISOCYANATE

  • Name: BENZENESULFONYL ISOCYANATE
  • CAS: 2845-62-7
  • Purity: 99%
  • Description

    Cost-effective customized wholesale BENZENESULFONYL ISOCYANATE 2845-62-7

    • Molecular Formula: C7H5NO3S
    • Molecular Weight: 183.188
    • Appearance/Colour: clear colourless liquid 
    • Vapor Pressure: 0.0104mmHg at 25°C 
    • Refractive Index: n20/D 1.536(lit.)  
    • Boiling Point: 272 °C at 760 mmHg 
    • Flash Point: 118.3 °C 
    • PSA: 71.95000 
    • Density: 1.31 g/cm3 
    • LogP: 1.79190 

    BENZENESULFONYL ISOCYANATE(Cas 2845-62-7) Usage

    General Description

    Benzenesulfonyl isocyanate reacts with ethanol and phenol to yield normal urethan products.

    InChI:InChI=1/C7H5NO3S/c9-6-8-12(10,11)7-4-2-1-3-5-7/h1-5H

    2845-62-7 Relevant articles

    Spiro-fysed 2-alkoxy-2-amino-Δ3-1,3,4-oxadiazolines. Synthesis and thermolysis to corresponding aminooxycarbenes

    Couture, Philippe,Warkentin, John

    , p. 1264 - 1280 (2007/10/03)

    Δ3-1,3,4-Oxadiazolines spiro-fused at C2...

    Unconventional Regiospecific Syntheses of Aromatic Carbonamides and Thiocarbonamides by Means of Tin-Mediated Friedel-Crafts Reactions

    Arnswald, Martin,Neumann, Wilhelm P.

    , p. 7022 - 7028 (2007/10/02)

    Friedel-Crafts reactions of stannylarene...

    Palladium-catalyzed carbonylation of (arylsulfonyliminoido)-benzenes to arylsulfonyl isocyanates

    Besenyei,Simandi

    , p. 2839 - 2842 (2007/10/02)

    In the presence of palladium complexes a...

    Mild and Efficient Synthesis of Aromatic Sulfonamides by in situ Preparation of the Corresponding Sulfonyl Isothiocyanates

    Arnswald, Martin,Neumann, Wilhelm P.

    , p. 1997 - 2000 (2007/10/02)

    A new reaction between chlorosulfonyl is...

    2845-62-7 Process route

    trimethylsilyl isocyanate
    1118-02-1

    trimethylsilyl isocyanate

    phenylsulfonyl fluoride
    368-43-4

    phenylsulfonyl fluoride

    trimethylsilyl fluoride
    420-56-4

    trimethylsilyl fluoride

    benzenesulphonyl isocyanate
    2845-62-7

    benzenesulphonyl isocyanate

    Conditions
    Conditions Yield
    With tin(IV) chloride; at 80 - 100 ℃; for 2h;
    93%
    N,N-bis(trimethylsilyl)benzenesulfonamide
    1023-95-6

    N,N-bis(trimethylsilyl)benzenesulfonamide

    benzenesulphonyl isocyanate
    2845-62-7

    benzenesulphonyl isocyanate

    Conditions
    Conditions Yield
    With phosgene; In diethyl ether; 8 h, at 0 deg C; 2 h, at 20 deg C;
    88%

    2845-62-7 Upstream products

    • 3315-16-0
      3315-16-0

      silver cyanate

    • 98-09-9
      98-09-9

      benzenesulfonyl chloride

    • 75-44-5
      75-44-5

      phosgene

    • 98-10-2
      98-10-2

      benzenesulfonamide

    2845-62-7 Downstream products

    • 22557-91-1
      22557-91-1

      N-(phenylcarbamoyl)benzenesulfonamide

    • 3559-04-4
      3559-04-4

      N-benzoyl-benzenesulfonamide

    • 22557-92-2
      22557-92-2

      N -acetyl-N '-benzenesulfonyl-urea

    • 5219-80-7
      5219-80-7

      N,N'-bis(benzenesulfonyl)urea

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