100306-33-0 | (R)-(+)-3-Chloro-1-phenyl-1-propanol

Packsize	Purity	Availability	Price	Discounted Price
5g	97%	in stock	$19.00	$13.00
10g	≥98%	in stock	$22.00	$15.00
25g	97%	in stock	$42.00	$30.00
100g	97%	in stock	$113.00	$79.00

Description

• Catalog Number: AA01829
• Chemical Name: (R)-(+)-3-Chloro-1-phenyl-1-propanol
• CAS Number: 100306-33-0
• Molecular Formula: C9H11ClO
• Molecular Weight: 170.6360
• MDL Number: MFCD00000463
• SMILES: ClCC[C@H](c1ccccc1)O

Computed Properties

• Complexity: 99.7
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 3
• XLogP3: 2

Upstream Synthesis Route

(R)-3-Chloro-1-phenylpropan-1-ol, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Due to its chiral nature, this compound serves as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its specific stereochemistry allows for the production of enantiopure products, which is essential in many industries where the biological activity or properties of a compound are dependent on its chirality.In chemical synthesis, (R)-3-Chloro-1-phenylpropan-1-ol can be utilized as a key starting material for the preparation of various biologically active molecules, such as chiral drugs and natural products. Its functional group allows for further derivatization, enabling the introduction of different chemical moieties to modify the properties of the final compound. Additionally, the presence of the chlorine atom and the phenyl group provides opportunities for diverse synthetic transformations, making it a valuable tool in the hands of synthetic chemists.Overall, the application of (R)-3-Chloro-1-phenylpropan-1-ol in chemical synthesis showcases its significance in designing and creating complex molecules with specific stereochemical requirements.

Literature

• Asymmetric synthesis of (S)-3-chloro-1-phenyl-1-propanol using Saccharomyces cerevisiae reductase with high enantioselectivity.

  Applied microbiology and biotechnology 20100601