15808-23-8

Basic information

• Product Name: 3,5-OCTADIYN-1,8-DIOL
• Synonyms: 3,5-OCTADIYN-1,8-DIOL;3,5-OCTADIYNE-1,8-DIOL;TIMTEC-BB SBB009113;octa-3,5-diyne-1,8-diol;3,5-OCTADIYN-1,8-DIOL, 96%,
• CAS NO: 15808-23-8
• Molecular Formula: C₈H₁₀O₂
• Molecular Weight: 138.16
• Mol File: 15808-23-8.mol
• Article Data: 12

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3,5-OCTADIYN-1,8-DIOL(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-OCTADIYN-1,8-DIOL(15808-23-8)
• EPA Substance Registry System: 3,5-OCTADIYN-1,8-DIOL(15808-23-8)

Safety Data

• Hazardous Substances Data: 15808-23-8(Hazardous Substances Data)

Usage

General Description

3,5-octadiyn-1,8-diol is a chemical compound with the molecular formula C8H10O2. It is a diol, meaning it contains two hydroxyl groups (-OH) attached to adjacent carbon atoms in the carbon chain. 3,5-OCTADIYN-1,8-DIOL is a colorless liquid at room temperature and is insoluble in water. It is primarily used in organic synthesis and as a building block for the production of various chemical compounds. Additionally, 3,5-octadiyn-1,8-diol has potential applications in the field of materials science, particularly as a precursor for the synthesis of polymers and other functional materials. 3,5-OCTADIYN-1,8-DIOL has also been studied for its potential pharmacological properties, showing promise in anti-inflammatory and antimicrobial applications.

Upstream product

• 927-74-2 3-Butyn-1-ol 
• 50360-48-0 1,8-bis-(1-butoxy-ethoxy)-octa-3,5-diyne 
• 64-17-5 ethanol 
• 3140-93-0 2,3-dibromothiophen 
• 386213-46-3 2-((E)-4-stilbenyl)-1,1-dibromoethene 
• 1160112-71-9 5-bromo-5'-iodo-1-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranos-1-yl)isoindigo 

Downstream Products

• 629-41-4 1,8-Octanediol 

Relevant articles and documents

In the optically-multiplexed-

A method for optical super-multiplexing using polyynes to provide enhanced images from stimulated Raman microscopy is disclosed. In some exemplary embodiments, the polyynes are organelle-targeted or spectral barcoded. Imaging can be enhanced by using the polyynes to image whole live cells or specific organelles within live cells. The polyynes can also be used in optical data storage (i.e., encoding) and identification (i.e., decoding) applications.

Good conductivity of a single component polydiacetylene film

Two films were prepared from single component monomer solutions. In these monomers, diacetylene and two acid groups are licked by flexible side chains. The side chain serves as the spacer between diacetylenes. After UV-irradiation, monomer films were transformed to polydiacetylene films and one of films exhibited conductivity drastically increases. This conductivity is two orders of magnitude greater than the conductivity value of reported nondoped polydiacetylene films.

Copper(i) chloride catalysed room temperature Csp-Csp homocoupling of terminal alkynes mediated by visible light

We developed a technique mediated by visible light for the aerobic homocoupling of terminal alkynes to synthesize 1,3-conjugated diynes using a copper(i) chloride catalyst at room temperature. Compared with previously reported thermal processes, this photochemical method is simple, uses only mild reaction conditions, produces high yields and works well for substrates with electron-withdrawing groups without the need for bases/ligands, oxidants or palladium catalysts.