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112747 Sigma-Aldrich

N-Acetylsulfanilyl chloride

98%

Synonym: 4-Acetamidobenzenesulfonyl chloride

  • CAS Number 121-60-8

  • Linear Formula 4-(CH3CONH)C6H4SO2Cl

  • Molecular Weight 233.67

  •  Beilstein/REAXYS Number 746676

  •  EC Number 204-485-1

  •  MDL number MFCD00007442

  •  PubChem Substance ID 24847112

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Properties

Related Categories Building Blocks, Chemical Synthesis, Organic Building Blocks, Sulfonyl Halides, Sulfur Compounds More...
assay   98%
mp   142-145 °C (dec.) (lit.)
SMILES string   CC(=O)Nc1ccc(cc1)S(Cl)(=O)=O
InChI   1S/C8H8ClNO3S/c1-6(11)10-7-2-4-8(5-3-7)14(9,12)13/h2-5H,1H3,(H,10,11)
InChI key   GRDXCFKBQWDAJH-UHFFFAOYSA-N

Description

General description

L-hydroxyproline has been derivatized with N-acetylsulfanilyl chloride and 5-chlorovaleric acid during the synthesis of the haptens HP1 and HP2.

Application

N-Acetylsulfanilyl chloride is used in the synthesis of N1,N1-dimethylsulfanilamide as the internal standard in the reaction. The reaction is used to determine tramadol and its O-desmethylated metabolite in blood plasma.

Packaging

1 kg in poly bottle

100 g in poly bottle

Safety & Documentation

Safety Information

Symbol 
Signal word 
Danger
Hazard statements 
Precautionary statements 
RIDADR 
UN 3261 8 / PGII
WGK Germany 
3
RTECS 
DB8837500

Documents

Certificate of Analysis (COA)

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Certificate of Origin (COO)

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Meet Synthia - Retrosynthesis Sofware
Protocols & Articles
Peer-Reviewed Papers
15

References

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