245365-64-4

Usage

Uses

Used in Pharmaceutical Industry:
N-CARBOBENZOXY-2-NITROBENZENESULFONAMIDE is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of Sulfanilamide-based drugs. Its presence in the synthesis process aids in the creation of a variety of pharmacologically active compounds that can be utilized for different medicinal purposes.
Used as a Reagent in Organic Synthesis:
In the field of organic chemistry, N-CARBOBENZOXY-2-NITROBENZENESULFONAMIDE is employed as a reagent. It plays a crucial role in various chemical reactions, facilitating the synthesis of complex organic molecules that can be used in a wide range of applications, from pharmaceuticals to other chemical industries.
Used in Other Industrial Applications:
Beyond its use in pharmaceuticals and organic synthesis, N-CARBOBENZOXY-2-NITROBENZENESULFONAMIDE may also have additional industrial applications. Its versatility and chemical properties make it a candidate for use in various sectors where specific chemical reactions or processes are required.

InChI:InChI=1/C14H12N2O6S/c17-14(22-10-11-6-2-1-3-7-11)15-23(20,21)13-9-5-4-8-12(13)16(18)19/h1-9H,10H2,(H,15,17)

Upstream product

• 5455-59-4 2-Nitrobenzenesulfonamide 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 245364-55-0 C₂₁H₂₆N₂O₆S 
• 1215685-54-3 tert-butyl (2R,5S,3E)-8-[N-(benzyloxycarbonyl)amino]-2-{3-[N-(benzyloxycarbonyl)-N-(o-nitrobenzenesulfonyl)amino]prop-1-yl}-5-[N-(o-nitrobenzenesulfonyl)amino]oct-3-enoate 
• 1186125-45-0 tert-butyl (2R,5S,3E)-2-{4-[N-(benzyloxycarbonyl)-N-(2-nitrophenylsulfonyl)amino]butyl}-9-[N-(2-chlorobenzyloxycarbonyl)amino]-5-[N-(2-nitrophenylsulfonyl)amino]non-3-enoate 
• 1214741-42-0 C₅₅H₅₂N₂O₁₁S 
• 1620387-64-5 C₂₇H₃₁FN₂O₁₀S 
• 1620387-57-6 C₁₆H₁₈FNO₄ 
• 1620387-66-7 C₂₁H₂₈FNO₆ 
• 245364-56-1 C₁₉H₂₀N₂O₈S 
• 1393524-11-2 benzyl (R)-but-3-yn-2-ylcarbamic acid 
• 1361407-81-9 tert-butyl (2S,5R,3E)-2-{3-[N-(benzyloxycarbonyl)amino]propyl}-5-[N-(tert-butoxycarbonyl)-amino]-6-(4-methoxyphenyl)-3,4-dimethylhex-3-enoate 
• 1333081-33-6 (2S,5R,3E)-2-{3-[N-(benzyloxycarbonyl)amino]propyl}-5-[N-(9-fluorenylmethoxycarbonyl)-amino]-6-(4-methoxyphenyl)-3,4-dimethylhex-3-enoic acid 

Relevant academic research and scientific papers

HEAVY-NITROGENIZED NITROBENZENESULFONAMIDE, ITS DERIVATIVE AND PRODUCTION METHOD THEREOF

PROBLEM TO BE SOLVED: To provide a heavy-nitrogenized nitrobenzenesulfonamide derivative and an efficient production method thereof. SOLUTION: The heavy-nitrogenized nitrobenzenesulfonamide compound is represented by general formula [2]. An amino group of

N-carboalkoxy-2-nitrobenzenesulfonamides: A practical preparation of N- Boc-, N-Alloc-, and N-Cbz-protected primary amines

N-Carboalkoxy-2-nitrobenzenesulfonamides, readily prepared by acylation of 2-nitrobenzenesulfonamide (o-NsNH2), can be alkylated by either conventional or Mitsunobu protocols. Since the o-nosyl group can be deprotected under mild conditions, a variety of N-carboalkoxy derivatives of primary amines may be prepared in excellent yields from the corresponding alcohols and/or halides. In addition, allyloxycarbonyl (Alloc), t- butoxycarbonyl (t-Boc), and benzyloxycarbonyl (Cbz) groups can be deprotected in the presence of the o-nosyl group, allowing the resultant N-alkylated 2- nitrobenzenesulfonamides to be used for further preparation of secondary amines.