Product Name:Tert-butyl ((5-bromothiazol-2-yl)methyl)carbamate

IUPAC Name:tert-butyl N-[(5-bromo-1,3-thiazol-2-yl)methyl]carbamate

CAS:713107-42-7
Molecular Formula:C9H13BrN2O2S
Purity:95%+
Catalog Number:CM428248
Molecular Weight:293.18

Packing Unit Available Stock Price($) Quantity
CM428248-100mg in stock ǤĽƓ
CM428248-250mg in stock ǵNJƓ
CM428248-500mg in stock NJƓǤ
CM428248-1g in stock ȎƓƓ
CM428248-5g in stock ǤŢƓƓ
CM428248-10g in stock ʼnƓƓƓ

For R&D use only.

Inquiry Form

   refresh    

Product Details

CAS NO:713107-42-7
Molecular Formula:C9H13BrN2O2S
Melting Point:-
Smiles Code:CC(C)(C)OC(=O)NCC1=NC=C(Br)S1
Density:
Catalog Number:CM428248
Molecular Weight:293.18
Boiling Point:
MDL No:
Storage:

Category Infos

Thiazoles
Thiazoles are very important functional groups in medicinal chemistry. They act as ligands on a variety of biological matrices. Thiazoles are used in a wide range of therapeutic applications, such as antibacterial, antiretroviral, antifungal, antiallergic, antihypertensive, pain treatment, and to control symptoms of schizophrenia.

Related Products



Product Other Information

Product Overview Tert-butyl ((5-bromothiazol-2-yl)methyl)carbamate, also known as TBBC, is an organic compound used in a variety of scientific research applications. TBBC is a brominated thiazole derivative that has been used for its wide range of properties, including its ability to form stable complexes with metal ions, its low toxicity, and its ability to act as a chelating agent. TBBC is a versatile compound that has been used in a variety of organic synthesis reactions, as well as in the study of biochemistry and physiology.
Synthesis and Application Tert-butyl ((5-bromothiazol-2-yl)methyl)carbamate can be synthesized in a variety of ways. The most common method of synthesis involves the reaction of tert-butyl bromide with 2-bromothiazole in the presence of a base such as sodium hydroxide or potassium hydroxide. The reaction is typically carried out in an aqueous solution at room temperature. Alternatively, Tert-butyl ((5-bromothiazol-2-yl)methyl)carbamate can be synthesized from the reaction of tert-butyl bromide with 5-bromo-2-methylthiazole in the presence of a base. Tert-butyl ((5-bromothiazol-2-yl)methyl)carbamate has been used in a variety of scientific research applications, including organic synthesis, biochemistry, and physiology. In organic synthesis, Tert-butyl ((5-bromothiazol-2-yl)methyl)carbamate has been used as a reagent for the synthesis of a variety of organic compounds, including cyclopropanes, cyclobutanes, and other heterocyclic compounds. In biochemistry, Tert-butyl ((5-bromothiazol-2-yl)methyl)carbamate has been used as a chelating agent for the study of metal ions and their interactions with proteins and other biomolecules. In physiology, Tert-butyl ((5-bromothiazol-2-yl)methyl)carbamate has been used to study the effects of metal ions on cell growth and development.
Future Directions Tert-butyl ((5-bromothiazol-2-yl)methyl)carbamate has a wide range of potential applications, both in research and in industry. In research, Tert-butyl ((5-bromothiazol-2-yl)methyl)carbamate could be used to study the effects of metal ions on proteins and other biomolecules, as well as the effects of metal ions on the immune system and nervous system. In industry, Tert-butyl ((5-bromothiazol-2-yl)methyl)carbamate could be used to develop new chelating agents for use in industrial processes. Additionally, Tert-butyl ((5-bromothiazol-2-yl)methyl)carbamate could be used to develop new methods for synthesizing organic compounds, as well as new methods for studying the effects of metal ions on cell growth and development.