N-(tert-Butoxycarbonyl)-2-nitrobenzenesulfonamide TCI B2303

Chemical Identity

CAS No.: 198572-71-3
PubChem: CID 11141172·SID 87565140
Formula: C11H14N2O6S
Molecular weight: 302.31 g/mol
Purity: >98.0%(HPLC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: tert-butyl N-(2-nitrophenyl)sulfonylcarbamate
SMILES: CC(C)(C)OC(=O)NS(=O)(=O)C1=CC=CC=C1[N+](=O)[O-]
InChIKey: WAYBGHIVTXTUCZ-UHFFFAOYSA-N

Rp 1.405.950,00

~~Rp 998.550,00~~ Rp 1.405.950,00

Sale Sold out

Shipping calculated at checkout.

Berat 1g 5g 25g

Pembayaran hanya melalui request quotation dan dilakukan setelah tim kami menghubungi Anda. Mohon cantumkan nomor WhatsApp aktif untuk konfirmasi pesanan & pembuatan invoice. Estimasi pengiriman 2-4 minggu setelah pembayaran.

Dokumen Keamanan & Mutu

↓ Unduh SDS / MSDS (PDF resmi TCI)

CoA (Certificate of Analysis)

Spesifik per batch produksi — diterbitkan dan dikirim bersama barang sesuai nomor lot yang Anda terima.

Contoh CoA segera tersedia.

💬 Minta CoA via WhatsApp

View full details

N-(tert-Butoxycarbonyl)-2-nitrobenzenesulfonamide is a synthetic reagent widely used in organic chemistry laboratories. This compound plays a crucial role in the formation of C-X bonds, specifically in non-halogen reactions, making it an essential tool for synthetic chemists. Its unique molecular structure allows it to participate in various chemical reactions, including substitution and electrophilic activation processes. As a versatile reagent, it is frequently employed in the synthesis of complex organic molecules, contributing to the development of new compounds and modifications of existing ones.

The compound is known for its chemical stability and predictable reactivity, which make it a preferred choice for laboratory use. Its ability to undergo controlled chemical transformations under specific conditions ensures reliable results in synthetic processes. Additionally, its compatibility with a range of reaction conditions and solvents enhances its utility in diverse chemical applications. These properties make it a reliable and efficient reagent for both academic and industrial research settings.

In Indonesian laboratories, N-(tert-Butoxycarbonyl)-2-nitrobenzenesulfonamide is commonly used in organic synthesis research. It is particularly relevant for chemists working in pharmaceutical and material science fields. Its application supports the development of new compounds and the optimization of existing chemical processes. Due to its stability and reactivity, it is a valuable resource for researchers aiming to advance their work in synthetic chemistry.

Advantages (TCI brochure)

o-Nitrobenzenesulfonyl (Ns) protected sulfonamide 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

TCI brochures (PDF)

Sulfonylation Reagents 2023-01-20 · p. 2
C-N Bond Formation Reactions 2025-08-07 · p. 2
Polyamines 2025-10-21 · p. 4

Related TCI products

Organic synthesis of complex molecules requiring substitution reactions due to its electrophilic activation properties
Development of new pharmaceutical compounds through controlled chemical transformations in laboratory settings
Modification of existing chemical structures in material science research for enhanced functional properties
Support for electrophilic substitution reactions in synthetic chemistry due to its stable molecular structure
Application in academic research for teaching and experimental purposes in chemical laboratories

From the TCI brochure

Synthesis of primary and secondary amines (Fukuyama method)

Brand	TCI
CAS number	198572-71-3
Molecular formula	—
Purity	—
Category	Chemistry > Synthetic Reagents > C-X(Non-Halogen) Bond Formation [Synthetic Reagents]
Pack sizes	Available in standard laboratory quantities
Physical form	Solid powder
Storage	Store in a cool, dry place away from direct sunlight

This compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its reactivity, it should be handled in a well-ventilated area, ideally with appropriate personal protective equipment. Avoid exposure to heat or direct light to preserve its integrity. Proper labeling and storage conditions ensure safe and effective use in laboratory settings. Always follow standard chemical safety protocols when working with this reagent.

—