1001648-73-2 | 2-Amino-6-bromo-5,6-dihydrobenzo[d]thiazol-7(4H)-one

Packsize	Purity	Availability	Price	Discounted Price
1mg		2 weeks	$105.00	$73.00
2mg		2 weeks	$123.00	$86.00
3mg		2 weeks	$149.00	$105.00
5mg		2 weeks	$168.00	$118.00
10mg		2 weeks	$193.00	$135.00

Description

• Catalog Number: AE14718
• Chemical Name: 2-Amino-6-bromo-5,6-dihydrobenzo[d]thiazol-7(4H)-one
• CAS Number: 1001648-73-2
• Molecular Formula: C7H7BrN2OS
• Molecular Weight: 247.1123
• MDL Number: MFCD19442517
• SMILES: BrC1CCc2c(C1=O)sc(=N)[nH]2

Computed Properties

• Complexity: 214
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• Undefined Atom Stereocenter Count: 1
• XLogP3: 2

Upstream Synthesis Route

2-Amino-6-bromo-5,6-dihydro-7(4H)-benzothiazolone is a versatile chemical compound widely utilized in chemical synthesis due to its unique properties and reactivity. One key application of this compound is its use as a building block in the synthesis of pharmaceutical intermediates and bioactive molecules.In organic synthesis, 2-Amino-6-bromo-5,6-dihydro-7(4H)-benzothiazolone serves as a valuable starting material for the construction of complex molecular structures. Its bromo functional group allows for further derivatization through various chemical reactions, enabling the introduction of different functional groups and modifications to tailor the compound for specific applications.Additionally, the presence of the amino group in 2-Amino-6-bromo-5,6-dihydro-7(4H)-benzothiazolone offers opportunities for selective reactions such as amine coupling, nucleophilic substitutions, and cyclization reactions. This enables chemists to access a diverse range of chemical transformations and synthetic pathways to access novel compounds with desired properties.Overall, the application of 2-Amino-6-bromo-5,6-dihydro-7(4H)-benzothiazolone in chemical synthesis opens up possibilities for the development of new drugs, agrochemicals, and advanced materials through strategic design and manipulation at the molecular level.