tert-butyl 4-[(6-nitro-1,3-benzothiazol-2-yl)carbamoyl]piperidine-1-carboxylate

Reagent Code: #238995
fingerprint
CAS Number 2507956-24-1

science Other reagents with same CAS 2507956-24-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 406.462 g/mol
Formula C₁₈H₂₂N₄O₅S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting enzyme inhibitors and receptor modulators. Its structure supports conjugation with biomolecules for assay development and labeling. Commonly employed in fluorescence-based applications due to the nitrobenzothiazole moiety, enabling detection in cellular imaging and diagnostic tools. Also utilized in the development of protease inhibitors and antimicrobial agents. Suitable for solid-phase and solution-phase peptide synthesis where protected functional groups are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿22,800.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-butyl 4-[(6-nitro-1,3-benzothiazol-2-yl)carbamoyl]piperidine-1-carboxylate
No image available

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting enzyme inhibitors and receptor modulators. Its structure supports conjugation with biomolecules for assay development and labeling. Commonly employed in fluorescence-based applications due to the nitrobenzothiazole moiety, enabling detection in cellular imaging and diagnostic tools. Also utilized in the development of protease inhibitors and antimicrobial agents. Suitable for solid

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting enzyme inhibitors and receptor modulators. Its structure supports conjugation with biomolecules for assay development and labeling. Commonly employed in fluorescence-based applications due to the nitrobenzothiazole moiety, enabling detection in cellular imaging and diagnostic tools. Also utilized in the development of protease inhibitors and antimicrobial agents. Suitable for solid-phase and solution-phase peptide synthesis where protected functional groups are required.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...