872-36-6 | 1,3-Dioxol-2-one

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$5.00	$4.00
25g	98%	in stock	$8.00	$6.00

Description

• Catalog Number: AB80359
• Chemical Name: 1,3-Dioxol-2-one
• CAS Number: 872-36-6
• Molecular Formula: C3H2O3
• Molecular Weight: 86.0462
• MDL Number: MFCD00005380
• SMILES: O=c1occo1

Computed Properties

• Complexity: 84.2
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 6
• Hydrogen Bond Acceptor Count: 3
• XLogP3: 0.3

Upstream Synthesis Route

Vinylene carbonate is a versatile compound known for its significance in chemical synthesis, particularly in the realm of polymer science. This unsaturated cyclic carbonate is widely utilized as a monomer in the production of various functional polymers and copolymers.In chemical synthesis, vinylene carbonate serves as a key building block for the synthesis of high-performance polymers such as poly(vinylene carbonate) and its copolymers. These polymers exhibit unique properties such as high conductivity, excellent thermal stability, and enhanced flexibility, making them valuable materials in a range of industrial applications.Additionally, vinylene carbonate plays a crucial role in the modification of polymer surfaces and the development of polymer electrolytes for advanced energy storage devices like lithium-ion batteries. Its ability to undergo copolymerization with other monomers allows for the creation of tailor-made polymer materials with specific properties suited for different applications.Furthermore, vinylene carbonate is an important intermediate in the production of functional additives, coatings, and adhesives due to its reactivity and compatibility with a variety of substrates. Its versatile nature and ability to undergo various chemical transformations make it a valuable component in the toolkit of synthetic chemists for designing innovative materials with tailored properties.

Literature

• Novel amides and esters prodrugs of olmesartan: Synthesis, bioconversion, and pharmacokinetic evaluation.

  Bioorganic & medicinal chemistry letters 20101001

• 3-(6-Benz-yloxy-2,2-dimethyl-perhydro-furo[2,3-d][1,3]dioxolan-5-yl)-5-(4-chloro-phen-yl)-4-nitro-2-phenyl-2,3,4,5-tetra-hydro-isoxazole.

  Acta crystallographica. Section E, Structure reports online 20091001

• Structural and vibrational studies of molecular conductors using quantum mechanical methods: 1,3-Dithiole-2-thione, 1,3-dithiole-2-one, 1,3-dioxole-2-one and 1,3-dioxole-2-thione.

  Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 20090915

• 3-(6-Benz-yloxy-2,2-dimethyl-perhydro-furo[2,3-d][1,3]dioxol-5-yl)-5-(4-bromo-phen-yl)-2-phenyl-perhydro-pyrrolo[3,4-d]isoxazole-4,6-dione.

  Acta crystallographica. Section E, Structure reports online 20090501

• End capping ring-opening olefin metathesis polymerization polymers with vinyl lactones.

  Journal of the American Chemical Society 20080820

• Supramolecular fluorophores for biological studies: phenylene vinylene-amino acid amphiphiles.

  Chemistry & biology 20051001

• Method for the rapid synthesis of highly functionalized 2-hydroxy-1-naphthoates. Syntheses of the naphthoic acid components of neocarzinostatin chromophore and N1999A2.

  Organic letters 20041125

• Immobilization of glucoamylase onto novel porous polymer supports of vinylene carbonate and 2-hydroxyethyl methacrylate.

  Applied biochemistry and biotechnology 20041101

• Chemoenzymatic synthesis and high-throughput screening of an aminoglycoside-polyamine library: identification of high-affinity displacers and DNA-binding ligands.

  Journal of the American Chemical Society 20041006

• Atomic force microscopy study on the stability of a surface film formed on a graphite negative electrode at elevated temperatures.

  Langmuir : the ACS journal of surfaces and colloids 20040217

• New supports for enzyme immobilization based on copolymers of vinylene carbonate and acrylamide.

  Applied biochemistry and biotechnology 20010701