502-44-3

  • Product Name:Epsilon-Caprolactone
  • Molecular Formula:C6H10O2
  • Purity:99%
  • Molecular Weight:114.144
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Product Details;

CasNo: 502-44-3

Molecular Formula: C6H10O2

Appearance: Clear colorless liquid, yellowing on ageing

Factory Export Top Purity Epsilon-Caprolactone 502-44-3 In Stock

  • Molecular Formula:C6H10O2
  • Molecular Weight:114.144
  • Appearance/Colour:Clear colorless liquid, yellowing on ageing 
  • Melting Point:-1 °C 
  • Refractive Index:n20/D 1.463(lit.)  
  • Boiling Point:225.393 °C at 760 mmHg 
  • Flash Point:84.805 °C 
  • PSA:26.30000 
  • Density:1.022 g/cm3 
  • LogP:1.10360 

2-Oxacycloheptanone(Cas 502-44-3) Usage

General Description

2-Oxacycloheptanone, also known as 2-oxocycloheptanone or 1,2-epoxy cycloheptanone, is a cyclic organic compound with a seven-membered ring and a ketone functional group. It is a colorless liquid with a pleasant odor and is widely used as an intermediate in the production of pharmaceuticals, perfumes, and other organic compounds. 2-Oxacycloheptanone is also utilized in the synthesis of polymers and as a solvent in various chemical reactions. It is known for its ability to undergo ring-opening reactions, making it an important building block in organic synthesis and drug development. Despite its synthetic importance, 2-oxacycloheptanone is not considered to be highly toxic or hazardous and has a relatively low risk of causing harm to human health or the environment.

InChI:InChI=1/C15H16Cl3N3O2.C6H10O2/c1-2-4-20(15(22)21-5-3-19-10-21)6-7-23-14-12(17)8-11(16)9-13(14)18;7-6-4-2-1-3-5-8-6/h3,5,8-10H,2,4,6-7H2,1H3;1-5H2

502-44-3 Relevant articles

Lipase catalysed oxidations in a sugar-derived natural deep eutectic solvent

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Chemoenzymatic oxidations involving the ...

Selective Aerobic Oxidation of Secondary C (sp3)-H Bonds with NHPI/CAN Catalytic System

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Cyclic ketones were quickly and quantita...

Aliphatic C–H hydroxylation activity and durability of a nickel complex catalyst according to the molecular structure of the bis(oxazoline) ligands

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502-44-3 Process route

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cyclohexanone

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toluene

hexahydro-2H-oxepin-2-one
502-44-3,24980-41-4,80137-66-2

hexahydro-2H-oxepin-2-one

benzaldehyde
100-52-7

benzaldehyde

benzoic acid
65-85-0,8013-63-6

benzoic acid

Conditions
Conditions Yield
With Iron(III) nitrate nonahydrate; N-hydroxyphthalimide; In acetonitrile; at 40 ℃; for 10h; under 1500.15 Torr; Temperature; Solvent; Large scale;
0.464 kg
1.76 kg
0.403 kg
7,15,16-Trioxa-dispiro[5.1.6.2]hexadecane
185614-71-5

7,15,16-Trioxa-dispiro[5.1.6.2]hexadecane

hexahydro-2H-oxepin-2-one
502-44-3,24980-41-4,80137-66-2

hexahydro-2H-oxepin-2-one

oxocan-2-one
539-87-7

oxocan-2-one

cyclohexanone
108-94-1,11119-77-0,9003-41-2,9075-99-4

cyclohexanone

cycloheptanone
502-42-1

cycloheptanone

Conditions
Conditions Yield
With titanium tetrachloride; at -78 ℃; Further Variations:; Reagents; Temperatures; Product distribution;
43%
5%
11%
41%

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