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CAS No 121-60-8 , 4-acetamidobenzenesulfonyl chloride

  • Name: 4-acetamidobenzenesulfonyl chloride
  • Synonyms: 121-60-8;4-acetamidobenzenesulfonyl chloride; Dagenan chloride; 4-Acetamidobenzenesulfonyl chloride;N-Acetylsulfanilyl chloride; 4-(ACETYLAMINO)BENZENESULFONYL CHLORIDE;
  • CAS Registry Number:
  • Transport: UN 3261
  • Melting Point: 145-148 ºC
  • Flash Point: 211.9 ºC
  • Boiling Point: 426.8 ºC at 760 mmHg
  • Density: 1.468 g/cm3
  • Refractive index: 1.586
  • Safety Statements: R34
  • Hazard Symbols: C: Corrosive;
  • HS Code: 29242995
  • Flash Point: 211.9 ºC
  • EINECS: 204-485-1
  • Molecular Weight: 233.67202
  • InchiKey: GRDXCFKBQWDAJH-UHFFFAOYSA-N
  • InChI: InChI=1S/C8H8ClNO3S/c1-6(11)10-7-2-4-8(5-3-7)14(9,12)13/h2-5H,1H3,(H,10,
    11)
  • Risk Statements: S26;S28B;S36/37/39;S45
  • Molecular Formula: C8H8ClNO3S
  • Molecular Structure:CAS No:121-60-8 4-acetamidobenzenesulfonyl chloride

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121-60-8 001 1-ACETAMIDOADAMANTANE

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121-60-8 ASC

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121-60-8 4-Acetamidobenzenesulfonyl chloride; 98%

  • 4-Acetamidobenzenesulfonyl chloride; 98%
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References of 4-acetamidobenzenesulfonyl chloride
Title: N-Acetylsulfanilyl Chloride
CAS Registry Number: 121-60-8
CAS Name: 4-(Acetylamino)benzenesulfonyl chloride
Synonyms: p-acetamidobenzenesulfonyl chloride; p-acetaminobenzenesulfonyl chloride; acetanilide-p-sulfonyl chloride; ASC
Molecular Formula: C8H8ClNO3S
Molecular Weight: 233.67
Percent Composition: C 41.12%, H 3.45%, Cl 15.17%, N 5.99%, O 20.54%, S 13.72%
Literature References: Prepd by sulfonation of acetanilide: Stewart, J. Chem. Soc. 121, 2558 (1922); Smiles, Stewart, Org. Synth. coll. vol. I, 8 (2nd ed., 1941).
Properties: Thick, light tan prisms from benzene, mp 149°. Has slight odor of acetic acid. Benzene and ether are poor solvents for purification by recrystn. Much better results are obtained using chloroform or ethylene dichloride. Cf. Northey, Sulfonamides (New York, 1948) p 12.
Melting point: mp 149°
CAUTION: Irritant to skin, eyes, and mucous membranes of nose and throat.
Use: Intermediate in the prepn of sulfanilamide and its derivs.