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4,5,6,7-Tetrahydroindene

  • CAS No.:24279-06-9
  • Purity:99%
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Manufacturer Supply Best Quality 4,5,6,7-Tetrahydroindene 24279-06-9 with Efficient Transportation

  • Molecular Formula:C9H12
  • Molecular Weight:120.194
  • Vapor Pressure:0.364mmHg at 25°C 
  • Boiling Point:205 ºC 
  • Flash Point:53 ºC 
  • PSA：0.00000 
  • Density:0.95 
  • LogP:2.81690 

4,5,6,7-Tetrahydroindene(Cas 24279-06-9) Usage

Synthesis Reference(s)

Tetrahedron Letters, 14, p. 4591, 1973 DOI: 10.1016/S0040-4039(01)87284-1

InChI:InChI=1/C9H12/c1-2-5-9-7-3-6-8(9)4-1/h3,6H,1-2,4-5,7H2

24279-06-9 Relevant articles

Corrigendum to: Ligand-Controlled Regiodivergent Pathways of Rhodium(III)-Catalyzed Dihydroisoquinolone Synthesis: Experimental and Computational Studies of Different Cyclopentadienyl Ligands (Chemistry - A European Journal, (2014), 20, 47, (15409-15418), 10.1002/chem.201404515)

Wodrich, Matthew D.,Ye, Baihua,Gonthier, Jér?me F.,Corminboeuf, Clémence,Cramer, Nicolai

supporting information, p. 7727 - 7727 (2020/06/16)

The authors became aware that product 4a...

Ligand-Controlled Regiodivergent Pathways of Rhodium(III)-Catalyzed Dihydroisoquinolone Synthesis: Experimental and Computational Studies of Different Cyclopentadienyl Ligands

Wodrich, Matthew D.,Ye, Baihua,Gonthier, Jér?me F.,Corminboeuf, Clémence,Cramer, Nicolai

supporting information, p. 15409 - 15418 (2016/02/18)

RhIII-catalyzed directed C-H functionali...

Easy access to (n+3)-dimethylamino-1-ethenylbicyclo[n.1.0]alkanes and their facile conversion to ring-annelated cyclopentadienes

Voigt, Tobias,Winsel, Harald,De Meijere, Armin

, p. 1362 - 1364 (2007/10/03)

Aminocyclopropanation of 1-ethenylcycloa...

Synthesis and properties of novel substituted 4,5,6,7-tetrahydroindenes and selected metal complexes

Austin, Rachel N.,Clark, T. Jeffrey,Dickson, Thomas E.,Killian, Christopher M.,Nile, Terence A.,et al.

, p. 11 - 18 (2007/10/02)

The synthesis of a complete series of su...

24279-06-9 Process route

tricyclo<4.3.0.0<sup>2,9</sup>>nonane
3103-88-6

tricyclo<4.3.0.02,9>nonane

bicyclo<4.3.0>nona-1(6),7-diene
24279-06-9

bicyclo<4.3.0>nona-1(6),7-diene

bicyclo<4.3.0>non-1(2)-ene
16189-42-7

bicyclo<4.3.0>non-1(2)-ene

1-vinylcyclopentene
28638-58-6

1-vinylcyclopentene

bicyclo<4.3.0>non-1(9)-ene
16189-41-6

bicyclo<4.3.0>non-1(9)-ene

Conditions
Conditions Yield
at 660 ℃; under 0.2 Torr;
44 % Chromat.
23 % Chromat.
10 % Chromat.
23 % Chromat.
C<sub>11</sub>H<sub>19</sub>NO

C11H19NO

bicyclo<4.3.0>nona-1(6),7-diene
24279-06-9

bicyclo<4.3.0>nona-1(6),7-diene

bicyclo<4.3.0>nona-6,9(1)-diene
24279-07-0

bicyclo<4.3.0>nona-6,9(1)-diene

Conditions
Conditions Yield
With water; at 150 ℃; under 1 Torr; Title compound not separated from byproducts;

24279-06-9 Upstream products

  • 3103-88-6
    3103-88-6

    tricyclo<4.3.0.02,9>nonane

  • 39832-95-6
    39832-95-6

    4,5,6,7-tetrahydro-1-indanol

  • 2622-21-1
    2622-21-1

    1-vinylcyclohexene

  • 5732-44-5
    5732-44-5

    1,3,2-dioxathiepane 2,2-dioxide

24279-06-9 Downstream products

  • 12113-37-0
    12113-37-0

    bis[η5-(4,5,6,7-tetrahydro-1H-indenyl)]titanium dichloride

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