N-Benzyloxycarbonyl-2-nitrobenzenesulfonamide TCI C1757

Chemical Identity

Other names: N-Cbz-2-nitrobenzenesulfonamide · N-Carbobenzoxy-2-nitrobenzenesulfonamide · Benzyl [(2-Nitrophenyl)sulfonyl]carbamate
CAS No.: 245365-64-4
PubChem: CID 10980593·SID 87566717
Formula: C14H12N2O6S
Molecular weight: 336.32 g/mol
Purity: >98.0%(HPLC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: benzyl N-(2-nitrophenyl)sulfonylcarbamate
SMILES: C1=CC=C(C=C1)COC(=O)NS(=O)(=O)C2=CC=CC=C2[N+](=O)[O-]
InChIKey: BFQXFHUTPNBFSR-UHFFFAOYSA-N
MDL: MDL06797080

Rp 2.730.000,00

~~Rp 1.924.650,00~~ Rp 2.730.000,00

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Berat 5g 25g

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N-Benzyloxycarbonyl-2-nitrobenzenesulfonamide is a synthetic reagent widely used in organic chemistry for the formation of C-X (non-halogen) bonds. This compound is known for its ability to participate in substitution reactions and molecular coupling processes, making it essential in the synthesis of complex organic compounds. Its stable structure allows it to react selectively with various reagents such as amines, acids, and bases. In laboratory applications, it is commonly used in research related to the development of bioactive compounds and pharmaceuticals. Due to its reactivity and specificity, this compound is a preferred choice for experiments requiring precision and controlled chemical reactions. Its versatility makes it a valuable tool for both academic and industrial research in Indonesia.

Advantages (TCI brochure)

o-Nitrobenzenesulfonyl (Ns) protected sulfonamide with Cbz group for amine synthesis
Protected amines formed with alkyl halides under basic conditions or with alcohols under Mitsunobu conditions
Each protecting group can be selectively removed