14860-69-6

Basic information

• Product Name: Benzenesulfonyl azide, 4-amino-
• CAS NO: 14860-69-6
• Molecular Formula: C6H6N4O2S
• Molecular Weight: 198.205
• Mol File: 14860-69-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzenesulfonyl azide, 4-amino-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonyl azide, 4-amino-(14860-69-6)
• EPA Substance Registry System: Benzenesulfonyl azide, 4-amino-(14860-69-6)

Safety Data

• Hazardous Substances Data: 14860-69-6(Hazardous Substances Data)

Upstream product

• 121-60-8 p-acetylaminobenzenesulfonyl chloride 
• 2158-14-7 4-acetamidobenzenesulfonyl azide 

Downstream Products

• 95469-97-9 5-oxo-1-sulfanilyl-2,5-dihydro-1H-[1,2,3]triazole-4-carboxylic acid ethyl ester; sodium-compound 
• 938-10-3 phenylsulfonyl azide 
• 63-74-1 sulfanilamide 
• 3563-14-2 4-{3-carboxy-propionylamino}-benzene-1-sulfonamide 
• 76464-66-9 N-(4-Azidosulfonylphenyl)-maleic acid monoamide 
• 93345-19-8 C₂₀H₂₈N₃O₈PS₂ 
• 93345-20-1 N-{4-[4-(3-Aza-tricyclo[3.2.1.0^2,4]octane-3-sulfonyl)-phenylsulfamoyl]-phenyl}-acetamide 
• 132994-81-1 4-(Azepine-1-sulfonyl)-phenylamine 
• 93345-18-7 4-(4-Acetylamino-benzenesulfonylamino)-benzenesulfonyl azide 
• 93101-08-7 1-cyclobutylmethylpiperidylidene-2-(4-aminophenyl)sulfonamide 
• 93101-05-4 4-Amino-N-[1-cyclopropylmethyl-piperidin-(2E)-ylidene]-benzenesulfonamide 
• 93101-14-5 4-Amino-N-[1-isobutyl-piperidin-(2E)-ylidene]-benzenesulfonamide 
• 93101-11-2 4-Amino-N-[1-propyl-piperidin-(2E)-ylidene]-benzenesulfonamide 
• 93100-95-9 4-Amino-N-[1-methyl-piperidin-(2E)-ylidene]-benzenesulfonamide 

Relevant articles and documents

Sulfonyl azide-mediated norbornene aziridination for orthogonal peptide and protein labeling

We describe a new bioconjugation reaction based on the aziridination of norbornenes using electron-deficient sulfonyl azides. The reaction enables to attach various useful tags to peptides and proteins under mild conditions. This journal is

POLYNUCLEOTIDE LABELING REAGENT

The present invention provides a new labeling reagent for preparing modified oligonucleotides and processes for their production wherein these oligonucleotides contain at least once the structure P═N—SO2-benzole-L-M-X, characterized in that L i

Syntheses of N4-(Alkyl or arylsulfonyl)sulfanilyl Derivatives

2,4-Dichloro, 2,5-dichloro and 3,4-dichloro-benzene-sulfanilides react with chlorosulfonic acid at low temperature to give good yields of the corresponding dichlorobenzenesulfonyl sulfanilyl chlorides.A number of chlorides have been converted into derivatives by reaction with nucleophiles, such as dimethylamine, hydrazine and sodium azide.N4-Acetamidobenzenesulfonylsulfanilyl derivatives have been prepared by the condensation of N4-acetylsulfanilyl chloride with the appropriate sulfanilyl derivative.Methylsulfonanilide reacts with chlorosulfonic acid to give N4-(methylsulfonyl)sulfanilyl chloride.The compounds have been tested for their antibacterial and antifungal activity.