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Home  > Chemistry  > Heterocyclic Building Blocks  > Tetrahydroquinolines  > 7-Bromo-1,2,3,4-tetrahydroquinoline

AA19422

114744-51-3 | 7-Bromo-1,2,3,4-tetrahydroquinoline

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $14.00 $10.00 -   +
5g 98% in stock $191.00 $134.00 -   +
10g 98% in stock $292.00 $205.00 -   +
25g 98% in stock $690.00 $483.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA19422
Chemical Name: 7-Bromo-1,2,3,4-tetrahydroquinoline
CAS Number: 114744-51-3
Molecular Formula: C9H10BrN
Molecular Weight: 212.0864
MDL Number: MFCD08544270
SMILES: Brc1ccc2c(c1)NCCC2

 

Computed Properties
Complexity: 138  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 1  
XLogP3: 3  

 

 

Upstream Synthesis Route
  • 7-Bromo-1,2,3,4-tetrahydroquinoline is a versatile compound widely utilized in chemical synthesis as a building block for the preparation of various heterocyclic derivatives. With its unique structure and reactivity, this compound plays a crucial role in the creation of pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 7-Bromo-1,2,3,4-tetrahydroquinoline serves as a key intermediate for the construction of more complex molecules. Its bromine functional group enables selective transformations through substitution and coupling reactions, allowing for precise modification of the quinoline core. This flexibility makes it a valuable tool for the synthesis of diverse molecular structures with potential applications in drug discovery and development.Moreover, the presence of the tetrahydroquinoline scaffold in this compound imparts specific properties to the resulting derivatives, making them ideal candidates for biological screening and optimization. By strategically incorporating 7-Bromo-1,2,3,4-tetrahydroquinoline into synthetic pathways, chemists can access novel compounds with enhanced bioactivity and selectivity, paving the way for the discovery of new therapeutic agents and chemical entities.Overall, the strategic application of 7-Bromo-1,2,3,4-tetrahydroquinoline in chemical synthesis enables chemists to explore innovative routes towards the development of biologically active compounds and advanced materials, driving progress in the fields of medicinal chemistry, agriculture, and materials science.
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