Safety of (2S)-(+)-3-Chloropropane-1,2-diol. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: (2S)-(+)-3-Chloropropane-1,2-diol, is researched, Molecular C3H7ClO2, CAS is 60827-45-4, about The male antifertility activity of 6-chloro-6-deoxyglucose. Author is Jones, A. R.; Dobbie, M. S..
6-Chloro-6-deoxy[U-14C]glucose is not metabolized by mature boar spermatozoa nor has it any specific inhibitory action on their metabolic activity in vitro. The compound is metabolized by the male rat and the identification of 2 urinary metabolites as α-chlorohydrin and 3-chlorolactate confirmed that (S)-3-chlorolactaldehyde is produced by this species in vivo. A tissue distribution study revealed that radioactivity from 6-chloro-6-deoxy[U-14C]glucose was more concentrated in rat caudal spermatozoa than in any other of the major tissues.
There is still a lot of research devoted to this compound(SMILES：OC[C@H](O)CCl)Safety of (2S)-(+)-3-Chloropropane-1,2-diol, and with the development of science, more effects of this compound(60827-45-4) can be discovered.
Reference:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com