structure of (1S)-1-[(2R)-Oxiran-2-yl]prop-2-en-1-ol

(1S)-1-[(2R)-Oxiran-2-yl]prop-2-en-1-ol

CAS No.: 100017-22-9
M. Wt: 100.11600
M. Fa: C5H8O2
InChI Key: YYUNQECXARGEAQ-CRCLSJGQSA-N
Appearance: Liquid

Names and Identifiers of (1S)-1-[(2R)-Oxiran-2-yl]prop-2-en-1-ol

CAS Number

100017-22-9

IUPAC Name

(1S)-1-[(2R)-oxiran-2-yl]prop-2-en-1-ol

InChI

InChI=1S/C5H8O2/c1-2-4(6)5-3-7-5/h2,4-6H,1,3H2/t4-,5+/m0/s1

InChIKey

YYUNQECXARGEAQ-CRCLSJGQSA-N

Canonical SMILES

C=CC(C1CO1)O

Isomeric SMILES

C=C[C@@H]([C@H]1CO1)O

Physical and chemical properties of (1S)-1-[(2R)-Oxiran-2-yl]prop-2-en-1-ol

Exact Mass

100.05200

Molecular Formula

C5H8O2

Molecular Weight

100.11600

PSA

32.76000

Solubility

DCM, Ethyl Acetate, Methanol

Safety Information of (1S)-1-[(2R)-Oxiran-2-yl]prop-2-en-1-ol

Pictograms

Signal Word

 Warning

Safety Data Sheet
Supports customized editing of SDS information and downloading in PDF documents.

Applications of (1S)-1-[(2R)-Oxiran-2-yl]prop-2-en-1-ol

(1S)-1-[(2R)-Oxiran-2-yl]prop-2-en-1-ol finds applications across various fields:

  • Organic Synthesis: It serves as an essential intermediate in synthesizing pharmaceuticals and agrochemicals.
  • Chiral Building Block: Its chirality makes it useful in asymmetric synthesis, where the creation of specific stereoisomers is crucial.

These applications underscore its significance in both research and industrial contexts.

Interaction Studies of (1S)-1-[(2R)-Oxiran-2-yl]prop-2-en-1-ol

Interaction studies involving (1S)-1-[(2R)-Oxiran-2-yl]prop-2-en-1-ol focus on its reactivity with biological targets. The compound's epoxide moiety is particularly reactive towards nucleophiles, including amino acids and proteins, which can lead to modifications that may alter biological functions. Understanding these interactions is vital for assessing its safety and efficacy in potential therapeutic applications.

Biological Activity of (1S)-1-[(2R)-Oxiran-2-yl]prop-2-en-1-ol

Research indicates that (1S)-1-[(2R)-Oxiran-2-yl]prop-2-en-1-ol exhibits notable biological activities. It has been studied for its potential antimicrobial properties and its role as an intermediate in the synthesis of biologically active compounds. The presence of the epoxide group is particularly significant, as epoxides are known for their ability to interact with biological macromolecules, potentially leading to therapeutic applications.

Retrosynthesis analysis of (1S)-1-[(2R)-Oxiran-2-yl]prop-2-en-1-ol

  • Route#1

    Cas:922-65-6
    Cas:100017-22-9