1445-91-6 | (S)-(-)-1-Phenylethanol

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$8.00	$5.00
5g	98%	in stock	$10.00	$7.00
10g	98%	in stock	$12.00	$8.00
25g	98%	in stock	$18.00	$12.00
100g	98%	in stock	$52.00	$36.00

Description

• Catalog Number: AI35825
• Chemical Name: (S)-(-)-1-Phenylethanol
• CAS Number: 1445-91-6
• Molecular Formula: C8H10O
• Molecular Weight: 122.1644
• MDL Number: MFCD00064264
• SMILES: C[C@@H](c1ccccc1)O

Computed Properties

• Complexity: 74.6
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 9
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 1.4

Upstream Synthesis Route

(S)-1-Phenylethanol, also known as (S)-alpha-methyl benzyl alcohol, is a chiral compound that plays a crucial role in various chemical synthesis reactions. Its stereochemistry, with the asymmetric carbon centered on the benzene ring, allows it to act as a versatile intermediate in organic chemistry processes.One key application of (S)-1-Phenylethanol in chemical synthesis is its use as a chiral building block for the preparation of enantiomerically pure compounds. Due to its chiral nature, (S)-1-Phenylethanol can be utilized in asymmetric synthesis to access specific enantiomers of target molecules. This compound serves as a valuable starting material in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where stereochemistry is crucial for biological activity or industrial applications.In addition, (S)-1-Phenylethanol can be employed in the synthesis of fragrances and flavors, contributing to the creation of unique scents and tastes in various consumer products. Its aromatic properties, combined with its chiral configuration, make it a desirable ingredient in the production of perfumes, cosmetics, and food additives.Overall, the application of (S)-1-Phenylethanol in chemical synthesis showcases its significance as a building block for the creation of diverse compounds with specific stereochemical characteristics, enabling the development of innovative products in the fields of pharmaceuticals, agrochemicals, fragrances, and flavors.

Literature

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• Germination and growth inhibitors from wheat (Triticum aestivum L.) husks.

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• Seasonal variation in leaf glucosinolates and insect resistance in two types of Barbarea vulgaris ssp. arcuata.

  Phytochemistry 20010901