蜂竞生物

(1R)-2-chloro-1-(4-chlorophenyl)ethan-1-ol

The compound you mentioned, (1R)-2-chloro-1-(4-chlorophenyl)ethan-1-ol, is a chiral molecule with the following structure:

• Chirality: The (1R) designation indicates that the carbon at position 1 is in the R configuration (based on the Cahn-Ingold-Prelog priority rules).
• Functional groups:
• A chloro group (–Cl) at position 2.
• A hydroxyl group (–OH) at position 1.
• A 4-chlorophenyl group (a benzene ring with a chlorine substituent at the para position) attached to the same carbon as the hydroxyl group.

Structure:

      Cl
       |
  Cl-C6H4-CH-CH2-Cl
       |
      OH

• The 1R configuration means that the priorities of the groups around the chiral center (carbon 1) are arranged in a clockwise manner when viewed from the side opposite the lowest-priority group (in this case, the hydrogen atom).

Key features:

1. Chiral center: Carbon 1 is chiral due to the four different substituents: –OH, –C6H4Cl, –CH2Cl, and –H.
2. Optical activity: The molecule is optically active because it is chiral and can rotate plane-polarized light.
3. Stereochemistry: The (1R) configuration is important for its biological activity and interactions with other chiral molecules.

If you need further details about its synthesis, reactivity, or applications, feel free to ask!

中国|杭州|桐庐|蜂竞生物fenjinbio.com | 联系：17767155726，E-mail:hwl5726@163.com