1-DECALONE

Cost-effective customized wholesale 1-DECALONE 4832-16-0

  • Molecular Formula: C10H16O
  • Molecular Weight: 152.236
  • Vapor Pressure: 0.03mmHg at 25°C 
  • Refractive Index: n20/D 1.492(lit.) 
  • Boiling Point: 244.5°Cat760mmHg 
  • Flash Point: 90.3°C 
  • PSA: 17.07000 
  • Density: 0.982g/cm3 
  • LogP: 2.54580 

1-DECALONE(Cas 4832-16-0) Usage

General Description

1-Decalones are bicyclic ketones with the molecular formula C10H16O, existing as cis- and trans-isomers. These compounds are structurally characterized by a fused cyclohexane-cyclohexanone ring system, often referred to as decahydronaphthalen-1-one or bicyclo[4.4.0]decan-2-one. They are used as intermediates in organic synthesis and fragrances due to their stable, saturated ring framework and ketone functionality. The cis and trans isomers exhibit distinct physical and chemical properties, influencing their reactivity and applications in stereoselective reactions.

InChI:InChI=1/C10H16O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h8-9H,1-7H2/t8-,9-/m0/s1

4832-16-0 Relevant articles

Ozonation of decalin as a model saturated cyclic molecule: A spectroscopic study

Bykov, Gennadii L.,Ershov, Boris G.,Krasovskiy, Vladimir G.,Kustov, Alexander L.,Kustov, Leonid M.,Panich, Nadezhda M.

, (2021/09/20)

Ozonolysis is used for oxidation of a mo...

Catalytic oxidation of alcohols using Fe-bTAML and NaClO: Comparing the reactivity of Fe(V)O and Fe(IV)O intermediates

Jana, Sandipan,Thomas, Jithin,Sen Gupta, Sayam

, p. 476 - 482 (2018/11/23)

We demonstrate the selective oxidation o...

Copper nanoparticles on hydrotalcite as a heterogeneous catalyst for oxidant-free dehydrogenation of alcohols

Mitsudome, Takato,Mikami, Yusuke,Ebata, Kaori,Mizugaki, Tomoo,Jitsukawa, Koichiro,Kaneda, Kiyotomi

supporting information; experimental part, p. 4804 - 4806 (2009/03/12)

We have developed a highly efficient het...

Oppenauer oxidation of secondary alcohols with 1,1,1-trifluoroacetone as hydride acceptor

Mello, Rossella,Martinez-Ferrer, Jaime,Asensio, Gregorio,Gonzalez-Nunez, Maria Elena

, p. 9376 - 9378 (2008/03/13)

(Chemical Equation Presented) 1,1,1-Trif...

4832-16-0 Process route

cis-decalin
493-01-6

cis-decalin

2-decalone
1579-21-1,5779-29-3,5779-30-6,16021-08-2,52079-67-1,91684-29-6,91684-30-9,143392-76-1,4832-17-1

2-decalone

1-decalone
4832-16-0

1-decalone

1-decalinol
529-32-8,207127-50-2,691892-12-3

1-decalinol

decahydronaphthalen-2-ol
825-51-4

decahydronaphthalen-2-ol

Conditions
Conditions Yield
With (pyridine-2-carboxylate)VO(O2)(H2O)2; In acetonitrile; at 20 ℃; for 3h; Further byproducts given;
3.7 % Chromat.
2.2 % Chromat.
2.4 % Chromat.
0.4 % Chromat.
cis-decalin
493-01-6

cis-decalin

1-decalone
4832-16-0

1-decalone

trans-decal-9-ol
1654-87-1

trans-decal-9-ol

1-decalinol
529-32-8,207127-50-2,691892-12-3

1-decalinol

decahydronaphthalen-2-ol
825-51-4

decahydronaphthalen-2-ol

Conditions
Conditions Yield
With (pyridine-2-carboxylate)VO(O2)(H2O)2; In acetonitrile; at 20 ℃; for 3h; Further byproducts given;
3.7 % Chromat.
2.4 % Chromat.
0.4 % Chromat.
1.0 % Chromat.

4832-16-0 Upstream products

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    1-decalinol

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    32166-40-8

    cis-1-decalone

  • 493-01-6
    493-01-6

    cis-decalin

  • 1205-19-2
    1205-19-2

    γ- <2-oxo-cyclohexyl> -buttersaeure-methylester

4832-16-0 Downstream products

  • 21370-71-8
    21370-71-8

    trans-1-decalone

  • 108984-83-4
    108984-83-4

    3-[4-(2,4-dinitro-phenylhydrazono)-octahydro-[4a]naphthyl]-propionitrile

  • 84571-81-3
    84571-81-3

    C23 H27 ClN2

  • 72967-96-5
    72967-96-5

    2-(p-Toluenesulfinyl)-1-decalone