5391-88-8 | 1-(4-Bromophenyl)ethanol

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$8.00	$5.00
5g	97%	in stock	$16.00	$11.00
10g	97%	in stock	$24.00	$17.00
25g	97%	in stock	$49.00	$35.00
250g	97%	in stock	$478.00	$335.00

Description

• Catalog Number: AB56565
• Chemical Name: 1-(4-Bromophenyl)ethanol
• CAS Number: 5391-88-8
• Molecular Formula: C8H9BrO
• Molecular Weight: 201.06046
• MDL Number: MFCD00004514
• SMILES: CC(c1ccc(cc1)Br)O
• NSC Number: 3223

Computed Properties

• Complexity: 97.4
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• Undefined Atom Stereocenter Count: 1
• XLogP3: 2.1

Upstream Synthesis Route

1-(4-Bromophenyl)ethanol is a versatile chemical compound commonly used in chemical synthesis for various applications. This compound plays a crucial role as a key building block in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and advanced materials.Its functional groups make it a valuable intermediate in the synthesis of complex organic molecules. The 4-bromophenyl moiety provides a site for further functionalization through various chemical reactions, allowing for the creation of diverse and intricate chemical structures.One common application of 1-(4-Bromophenyl)ethanol is in the production of pharmaceutical compounds. By utilizing this compound as a starting material, chemists can introduce specific functional groups to tailor the properties of the final pharmaceutical product. Additionally, its versatility allows for the modification of molecular structures to enhance biological activity or improve drug efficacy.Furthermore, 1-(4-Bromophenyl)ethanol serves as a valuable synthetic building block in the development of agrochemicals. Its ability to undergo diverse chemical transformations enables the synthesis of novel pesticide and herbicide compounds with improved efficiency and selectivity in agricultural applications.Overall, the utility of 1-(4-Bromophenyl)ethanol in chemical synthesis extends to various industries, offering a flexible and reliable foundation for the creation of complex molecules with specific properties and applications.

Literature

• Didymosphaeria igniaria: a new microorganism useful for the enantioselective reduction of aryl-aliphatic ketones.

  Journal of industrial microbiology & biotechnology 20101101

• [Crystallization and structural investigation of supramolecular compounds with modified cyclodextrins. Application to chiral discrimination].

  Annales pharmaceutiques francaises 20100701

• Production of (R)-1-(4-Bromo-phenyl)-ethanol by locally isolated Aspergillus niger using ram horn peptone.

  Bioresource technology 20080401

• Chiral discrimination in host-guest supramolecular complexes. Understanding enantioselectivity and solid solution behaviors by using spectroscopic methods and chemical sensors.

  The journal of physical chemistry. B 20070628

• Enantioseparation on mono(6A-n-allylamino-6A-deoxy)permethylated 3-cyclodextrin covalently bonded silica gel.

  Journal of chromatography. A 20041203