141381-72-8

Basic information

• Product Name: 1H-benzo[d][1,2,3]triazol-1-yl 2-nitrobenzenesulfonate
• Synonyms: 1H-benzo[d][1,2,3]triazol-1-yl 2-nitrobenzenesulfonate
• CAS NO: 141381-72-8
• Molecular Weight: 320.285
• Mol File: 141381-72-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-benzo[d][1,2,3]triazol-1-yl 2-nitrobenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-benzo[d][1,2,3]triazol-1-yl 2-nitrobenzenesulfonate(141381-72-8)
• EPA Substance Registry System: 1H-benzo[d][1,2,3]triazol-1-yl 2-nitrobenzenesulfonate(141381-72-8)

Safety Data

• Hazardous Substances Data: 141381-72-8(Hazardous Substances Data)

Upstream product

• 2592-95-2 benzotriazol-1-ol 
• 1694-92-4 2-Nitrobenzenesulfonyl chloride 

Downstream Products

• 17606-70-1 (4Z)-4-benzylidene-2-phenyl-1,3-oxazol-5(4H)-one 
• 215056-52-3 N-2-nitrobenzenesulfonamideglycine methyl ester 
• 42060-32-2 N-benzyl-2-nitrobenzenesulfonamide 
• 54769-36-7 N-benzoyloxybenzotriazole 
• 141381-74-0 (E)-3-(4-Methoxy-phenyl)-acrylic acid benzotriazol-1-yl ester 
• 141381-81-9 phenylethylamide of o-nitrophenylsulfonic acid 
• 141381-73-9 Diphenyl-acetic acid benzotriazol-1-yl ester 

Relevant articles and documents

Synthesis of O-benzyl hydroxamates employing the sulfonate esters of N-hydroxybenzotriazole

The direct conversion of various carboxylic acids, that include sterically hindered amino acids and di-peptides, to O-benzyl hydroxamates is demonstrated using sulfonate esters of benzotriazoles under ambient and milder conditions without significant race

Differentially-protected steroidal triamines; scaffolds with potential for medicinal, supramolecular, and combinatorial chemistry

Cholic acid 2a has been converted into two new orthogonally-protected triamino scaffolds, 13 and 14. The synthesis proceeds via the bis-Boc-NH-substituted azide 10, for which an improved preparation is described. After removal of the Boc groups, the two a