10160-24-4 | 7-Bromo-1-heptanol

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$8.00	$5.00
1g	98%	in stock	$13.00	$9.00
5g	98%	in stock	$18.00	$12.00
10g	98%	in stock	$30.00	$21.00
25g	98%	in stock	$60.00	$42.00
100g	98%	in stock	$230.00	$161.00

Description

• Catalog Number: AA06203
• Chemical Name: 7-Bromo-1-heptanol
• CAS Number: 10160-24-4
• Molecular Formula: C7H15BrO
• Molecular Weight: 195.0974
• MDL Number: MFCD00041708
• SMILES: OCCCCCCCBr

Computed Properties

• Complexity: 48.2
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 6
• XLogP3: 2.3

Upstream Synthesis Route

7-Bromo-1-heptanol is a versatile compound that finds wide application in chemical synthesis due to its unique reactivity and structure. As a primary alcohol with a bromine atom attached to the seventh carbon, this compound serves as a valuable building block in the preparation of various organic molecules and compounds.In organic synthesis, 7-Bromo-1-heptanol can be used as a starting material for the synthesis of complex molecules such as pharmaceuticals, agrochemicals, and advanced materials. Its primary alcohol group allows for further derivatization through various chemical reactions, including esterification, oxidation, and reduction. The bromine atom imparts additional reactivity, enabling selective functionalization at the seventh carbon position.One common application of 7-Bromo-1-heptanol is in the synthesis of biologically active compounds or intermediates. By incorporating this compound into a synthesis route, chemists can introduce specific functionalities or structural motifs that are essential for the desired biological activity. Additionally, the bromine atom can function as a leaving group in substitution reactions, facilitating the construction of more complex molecular scaffolds.Overall, the strategic use of 7-Bromo-1-heptanol in chemical synthesis opens up new opportunities for creating novel compounds with diverse applications in the fields of medicine, agriculture, and materials science. Its versatility and reactivity make it a valuable tool for chemists seeking to develop innovative molecules with tailored properties and functions.

Literature

• Sequential substitution of 1,2-dichloro-ethene: a convenient stereoselective route to (9Z,11E)-, (10E,12Z)- and (10Z,12Z)-.

  Chemistry and physics of lipids 20010301