4541-14-4 | 4-Benzyloxy-1-butanol

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$10.00	$7.00
5g	97%	in stock	$11.00	$8.00
10g	97%	in stock	$20.00	$14.00
25g	97%	in stock	$40.00	$28.00
100g	97%	in stock	$136.00	$95.00

Description

• Catalog Number: AB66734
• Chemical Name: 4-Benzyloxy-1-butanol
• CAS Number: 4541-14-4
• Molecular Formula: C11H16O2
• Molecular Weight: 180.2435
• MDL Number: MFCD00155211
• SMILES: OCCCCOCc1ccccc1

Computed Properties

• Complexity: 109
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 6
• XLogP3: 1.6

Upstream Synthesis Route

4-(Benzyloxy)butan-1-ol, also known as benzyl 4-hydroxybutyrate, is a versatile compound widely used in various chemical synthesis processes. This compound plays a crucial role as a building block in the creation of complex organic molecules and pharmaceutical intermediates. Its unique structure allows for strategic functionalization and modification, making it a valuable asset in the hands of synthetic chemists.One key application of 4-(Benzyloxy)butan-1-ol is in the synthesis of esters, ethers, and other functionalized organic compounds. By utilizing its benzyl-protected hydroxyl group, chemists can selectively manipulate its reactivity to introduce new functional groups at specific positions along the molecular chain. This controlled modification capability is essential in the design and development of new drug candidates, agrochemicals, and specialty chemicals.Furthermore, 4-(Benzyloxy)butan-1-ol serves as a pivotal intermediate in the preparation of biologically active molecules such as pharmaceuticals, natural products, and fine chemicals. Its incorporation into complex structures allows for the introduction of diverse pharmacophores and substituents, enhancing the potency, selectivity, and bioavailability of the final products.In conclusion, the use of 4-(Benzyloxy)butan-1-ol in chemical synthesis offers chemists a powerful tool for building molecular diversity, designing novel compounds, and advancing the frontiers of organic chemistry. Its versatility and reactivity make it a valuable asset in the arsenal of synthetic methodologies, paving the way for innovation and discovery in the field of chemical sciences.

Literature

• Synthesis of (R)-2-methyl-4-deoxy and (R)-2-methyl-4,5-dideoxy analogues of 6-phosphogluconate as potential inhibitors of 6-phosphogluconate dehydrogenase.

  Organic & biomolecular chemistry 20030207