1038919-63-9 | (R)-5-Bromo-2,3-dihydro-1h-inden-1-ol

Packsize	Purity	Availability	Price	Discounted Price
250mg	96%	in stock	$139.00	$97.00
1g	95%	in stock	$289.00	$202.00
5g	95%	in stock	$1,063.00	$744.00

Description

• Catalog Number: AI06193
• Chemical Name: (R)-5-Bromo-2,3-dihydro-1h-inden-1-ol
• CAS Number: 1038919-63-9
• Molecular Formula: C9H9BrO
• Molecular Weight: 213.0712
• MDL Number: MFCD15529783
• SMILES: Brc1ccc2c(c1)CC[C@H]2O

Computed Properties

• Complexity: 149
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• XLogP3: 2.2

Upstream Synthesis Route

Application:
(R)-5-Bromo-2,3-dihydro-1H-inden-1-ol is a versatile compound widely utilized in chemical synthesis processes. Due to its unique structure, this compound serves as a valuable building block in the creation of various complex organic molecules. In particular, its bromine substituent and indenol backbone play crucial roles in diversifying chemical reactions and enabling the formation of structurally diverse compounds.One prominent application of (R)-5-Bromo-2,3-dihydro-1H-inden-1-ol is in the synthesis of chiral ligands and catalysts. The chirality of this compound imparts specific stereochemical properties that are essential in asymmetric synthesis, where the control of stereochemistry is of utmost importance. By incorporating this compound into ligand design, researchers can tailor catalysts for enantioselective reactions, leading to the production of single enantiomer products with high stereoselectivity.Furthermore, (R)-5-Bromo-2,3-dihydro-1H-inden-1-ol can also be employed in the construction of biologically active molecules. Its structural motifs provide opportunities for the design and synthesis of pharmaceutical intermediates, natural product derivatives, and novel chemical entities with potential therapeutic applications. The bromine functionality can serve as a handle for further elaboration through cross-coupling reactions, functional group transformations, and other synthetic manipulations, enabling the creation of diverse molecular architectures.Overall, the strategic incorporation of (R)-5-Bromo-2,3-dihydro-1H-inden-1-ol in chemical synthesis offers a pathway for accessing complex molecules with defined stereochemistry and functional diversity, making it a valuable resource for synthetic chemists seeking to expand the frontiers of molecular design and organic synthesis.