structure of Prenyl formate

Prenyl formate

CAS No.: 68480-28-4
M. Wt: 114.14200
M. Fa: C6H10O2
InChI Key: ZCROFVOAWLRGFY-UHFFFAOYSA-N

Names and Identifiers of Prenyl formate

CAS Number

68480-28-4

EC Number

270-906-0

IUPAC Name

3-methylbut-2-enyl formate

InChI

InChI=1S/C6H10O2/c1-6(2)3-4-8-5-7/h3,5H,4H2,1-2H3

InChIKey

ZCROFVOAWLRGFY-UHFFFAOYSA-N

Canonical SMILES

CC(=CCOC=O)C

UNII

77XFK1MOL6

Physical and chemical properties of Prenyl formate

Boiling Point

139.6ºC at 760mmHg

Density

0.920-0.927

Exact Mass

114.06800

Flash Point

41.4ºC

Index of Refraction

1.410-1.415

LogP

1.76150

Molecular Formula

C6H10O2

Molecular Weight

114.14200

PSA

26.30000

Solubility

Soluble (in ethanol)

Applications of Prenyl formate

Prenyl formate has several applications across different fields:

  • Pharmaceuticals: Its derivatives are explored for their potential use in drug development due to their biological activities.
  • Natural Products Chemistry: It serves as an important building block in synthesizing more complex natural products.
  • Agricultural Chemistry: Compounds derived from prenylated structures may exhibit pest-repellent properties or enhance plant resistance against pathogens.

Interaction Studies of Prenyl formate

Studies on the interactions of prenylated compounds reveal that they can modulate various biological pathways. For example:

  • Prenylated flavonoids have been shown to interact with cellular signaling pathways involved in inflammation and cancer progression.
  • They may also influence enzyme activities related to metabolic processes, such as α-glucosidase inhibition, which has implications for diabetes management.

Biological Activity of Prenyl formate

Prenylated compounds, including prenyl formate, exhibit a range of biological activities. Research indicates that prenylated flavonoids possess significant antioxidant properties, which contribute to their potential therapeutic effects against various diseases. Notably, these compounds have been studied for their anticancer, anti-inflammatory, and antimicrobial activities. The presence of the prenyl group often enhances the bioactivity compared to non-prenylated counterparts due to improved lipophilicity and cellular uptake.

Retrosynthesis analysis of Prenyl formate

  • Route#1

    Cas:141-53-7
    Cas:503-60-6
    Cas:64-18-6
    Cas:68480-28-4
  • Route#2

    Cas:556-82-1
    Cas:64-18-6
    Cas:68480-28-4
  • Route#3

    Cas:115-18-4
    Cas:64-18-6
    Cas:68480-28-4