9-Anthraceneacrylic acid

Base Information

Chemical Name:9-Anthraceneacrylic acid
CAS No.:5335-33-1
Molecular Formula:C17H12O2
Molecular Weight:248.281
Hs Code.:
NSC Number:2930
Nikkaji Number:J1.272.807G
Mol file:5335-33-1.mol

Synonyms:9-Anthraceneacrylic acid;5335-33-1;(E)-3-(ANTHRACEN-9-YL)ACRYLIC ACID;3-(9-Anthryl)propenoic acid;3-(Anthracen-9-yl)acrylic acid;(2E)-3-(ANTHRACEN-9-YL)PROP-2-ENOIC ACID;202998-44-5;(E)-3-anthracen-9-ylprop-2-enoic acid;NSC2930;NSC-2930;CS-0182972;J-650058

Suppliers and Price of 9-Anthraceneacrylic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 7 raw suppliers

Chemical Property of 9-Anthraceneacrylic acid

Chemical Property:

Vapor Pressure:2.59E-10mmHg at 25°C
Boiling Point:487.4°C at 760 mmHg
Flash Point:371°C
Density:1.284g/cm³
XLogP3:4.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:248.083729621
Heavy Atom Count:19
Complexity:338

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=C3C=CC=CC3=C2C=CC(=O)O
Isomeric SMILES:C1=CC=C2C(=C1)C=C3C=CC=CC3=C2/C=C/C(=O)O
General Description (2E)-3-anthracen-9-ylprop-2-enoic acid, also known as (E)-3-(anthracen-9-yl)acrylic acid (9-AYAA), is a photomechanically active organic compound that exhibits strong mechanical responses to light, such as coiling and uncoiling in microcrystalline form. While bulk crystals of 9-AYAA demonstrate notable photomechanical behavior, growing high-quality microcrystals has proven challenging through conventional methods like sublimation or reprecipitation. However, a chemical reaction-growth approach using its tert-butyl ester precursor enables the production of uniform microwires via acid-catalyzed hydrolysis. These microwires respond dynamically to 475 nm light, undergoing reversible structural transitions, highlighting their potential for photomechanical applications. The method’s success depends on reaction conditions, including temperature, surfactant concentration, and mixing mode.

Technology Process of 9-Anthraceneacrylic acid

There total 12 articles about 9-Anthraceneacrylic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.0%