4117-10-6 | 6-Hepten-1-ol

Packsize	Purity	Availability	Price	Discounted Price
250mg	95%	in stock	$38.00	$26.00
1g	95%	in stock	$86.00	$60.00
5g	95%	in stock	$206.00	$144.00
25g	95%	in stock	$884.00	$619.00

Description

• Catalog Number: AB69868
• Chemical Name: 6-Hepten-1-ol
• CAS Number: 4117-10-6
• Molecular Formula: C7H14O
• Molecular Weight: 114.1855
• MDL Number: MFCD00229167
• SMILES: OCCCCCC=C

Computed Properties

• Complexity: 50.3
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 5
• XLogP3: 1.9

Upstream Synthesis Route

6-Hepten-1-ol, also known as hept-6-en-1-ol, is a versatile compound widely utilized in chemical synthesis. This unsaturated alcohol plays a crucial role in numerous chemical reactions and processes due to its unique chemical properties. In the field of organic chemistry, 6-Hepten-1-ol is commonly employed as a starting material for the synthesis of various valuable compounds.One of the primary applications of 6-Hepten-1-ol is in the production of fragrances and aroma compounds. Its distinct odor profile, characterized by floral and fruity notes, makes it a popular choice for perfumery and flavor industries. By undergoing different chemical transformations, 6-Hepten-1-ol can be converted into fragrance ingredients that mimic natural scents or create entirely new olfactory experiences.Additionally, 6-Hepten-1-ol serves as a building block in the synthesis of fine chemicals and pharmaceuticals. Its reactive double bond and hydroxyl group make it a versatile intermediate for forming complex molecular structures. Chemists can functionalize 6-Hepten-1-ol through oxidation, reduction, or other chemical reactions to introduce specific functional groups required for the target compound synthesis.In organic synthesis, 6-Hepten-1-ol can participate in various transformations such as oxidation to the corresponding aldehyde or carboxylic acid, reduction to the corresponding alkane, or reaction with different electrophiles to form new carbon-carbon bonds. Its unsaturated nature provides opportunities for selective chemical modifications, enabling the creation of diverse molecules with tailored properties.Overall, 6-Hepten-1-ol's versatility and reactivity make it a valuable asset in chemical synthesis, offering a wide range of possibilities for creating novel compounds in industries ranging from fragrance and flavor to pharmaceuticals and fine chemicals.

Literature

• Synthesis of (1R,7Z)-1-methyl-7-hexadecenyl acetate, the female sex pheromone of the honey locust gall midge.

  Bioscience, biotechnology, and biochemistry 20120101