3360-41-6 | 4-Phenyl-1-butanol

Packsize	Purity	Availability	Price	Discounted Price
5g	97%	in stock	$10.00	$7.00
10g	97%	in stock	$14.00	$10.00
25g	97%	in stock	$17.00	$12.00
100g	97%	in stock	$52.00	$36.00
500g	97%	in stock	$242.00	$169.00

Description

• Catalog Number: AB45129
• Chemical Name: 4-Phenyl-1-butanol
• CAS Number: 3360-41-6
• Molecular Formula: C10H14O
• Molecular Weight: 150.2176
• MDL Number: MFCD00002971
• SMILES: OCCCCc1ccccc1
• NSC Number: 71383

Computed Properties

• Complexity: 84.9
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 4
• XLogP3: 2.3

Upstream Synthesis Route

4-Phenyl-1-butanol, a versatile compound widely used in chemical synthesis, serves as a valuable building block in various industrial processes. As a primary alcohol with a phenyl group attached to the carbon chain, it plays a crucial role in the creation of pharmaceuticals, fragrances, and fine chemicals. In the realm of organic chemistry, this compound is utilized for its ability to undergo a range of reactions, including oxidation, reduction, and esterification, enabling the production of diverse molecules. Moreover, its structural flexibility allows for the incorporation of the phenyl moiety into complex organic frameworks, enhancing the properties of the final products. With its significance in synthetic chemistry, 4-Phenyl-1-butanol continues to be a fundamental component in the development of innovative chemical compounds with various applications across industries.

Literature

• Novel free paclitaxel-loaded poly(L-γ-glutamylglutamine)-paclitaxel nanoparticles.

  International journal of nanomedicine 20110101

• Polymeric micelles in anticancer therapy: targeting, imaging and triggered release.

  Pharmaceutical research 20101201

• NK105, a paclitaxel-incorporating micellar nanoparticle, is a more potent radiosensitising agent compared to free paclitaxel.

  British journal of cancer 20060904

• Enhancing effect of alpha-hydroxyacids on 'in vitro' permeation across the human skin of compounds with different lipophilicity.

  International journal of pharmaceutics 20060511

• Isolation and functional analysis of cytochrome P450 CYP153A genes from various environments.

  Bioscience, biotechnology, and biochemistry 20051201

• NK105, a paclitaxel-incorporating micellar nanoparticle formulation, can extend in vivo antitumour activity and reduce the neurotoxicity of paclitaxel.

  British journal of cancer 20050411

• Novel CuS nanofibers using organogel as a template: controlled by binding sites.

  Langmuir : the ACS journal of surfaces and colloids 20041207

• Simple synthesis of beta-D-glycopyranosides using beta-glycosidase from almonds.

  Chemical & pharmaceutical bulletin 20040201