Monomers

Tributyl(3-ethenylphenyl)stannane

Identifiers

IUPAC name
tributyl-(3-ethenylphenyl)stannane
InchI
InChI=1S/C8H7.3C4H9.Sn/c1-2-8-6-4-3-5-7-8;3*1-3-4-2;/h2-4,6-7H,1H2;3*1,3-4H2,2H3;
InchI Key
ALUDIPIYKNWWLM-UHFFFAOYSA-N
SMILES
CCCC[Sn](c1cccc(c1)C=C)(CCCC)CCCC
Canonical SMILES
CCCC[Sn](CCCC)(CCCC)C1=CC=CC(=C1)C=C
Isomeric SMILES
CCCC[Sn](CCCC)(CCCC)C1=CC=CC(=C1)C=C
Resources

Structures

2D Structure
3D Structure

Molecular Formula and Computed Descriptors

Molecular Formula
C20H34Sn
Heavy Atom Count
21
Molecular Weight
393.203
Exact Molecular Weight
394.1682
Valence Electrons
118
Radical Electrons
0
tPSA
0.0
MolLogP
6.3857
H Bond Acceptors
0
H Bond Donors
0
Aliphatic Carbocycles
0
Aromatic Carbocycles
1
Aliphatic Heterocycles
0
Aromatic Heterocycles
0
Aliphatic Rings
0
Aromatic Rings
1

MOL File


     RDKit          3D

 55 55  0  0  0  0  0  0  0  0999 V2000
    0.3857   -4.5388    2.7272 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9034   -4.2912    1.3435 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9283   -2.7885    1.0413 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4861   -2.2201    1.1496 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3703   -0.1176    0.7144 Sn  0  0  0  0  0  4  0  0  0  0  0  0
    1.2220    0.1397   -0.6760 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1036   -0.5562   -1.8688 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0698   -0.4611   -2.8292 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1734    0.3596   -2.5627 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3005    1.0540   -1.3831 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2923    0.9364   -0.4160 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4408    1.8955   -1.1200 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4085    2.0357   -1.9956 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1541    0.5638   -0.2388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8552   -0.5316   -0.9893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1019    0.0893   -1.6155 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8715   -0.9797   -2.4019 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0527    1.0288    2.4718 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6811    2.3995    2.3515 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0894    3.1637    1.1852 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6986    4.5323    1.0446 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7217   -4.3834    2.6980 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6541   -5.5831    3.0101 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8441   -3.7817    3.3965 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2134   -4.7227    0.5693 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9134   -4.6997    1.1989 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6395   -2.2594    1.6959 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3049   -2.7056    0.0035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0849   -2.7448    0.3631 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8808   -2.4030    2.1649 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.2513   -1.1859   -2.0669 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9758   -1.0058   -3.7612 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8980    0.3891   -3.3631 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3474    1.4545    0.5109 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4997    2.4219   -0.1819 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4538    1.5636   -2.9530 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2772    2.6848   -1.7796 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8503    0.9938    0.4958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8940    1.3512   -0.9758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1233   -1.4018   -0.3628 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2516   -0.9287   -1.8311 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8276    0.8570   -2.3669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7381    0.5773   -0.8702 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4472   -1.0512   -3.4076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7770   -1.9204   -1.8191 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9196   -0.6097   -2.4512 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0160    1.1045    2.7482 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5510    0.5158    3.3302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6178    2.9724    3.2953 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7643    2.2700    2.1400 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9955    3.2413    1.3707 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2628    2.6297    0.2338 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7834    4.4910    0.9493 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2298    5.0083    0.1567 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4260    5.1474    1.9275 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 12 13  2  3
  5 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
  5 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 11  6  1  0
  1 22  1  0
  1 23  1  0
  1 24  1  0
  2 25  1  0
  2 26  1  0
  3 27  1  0
  3 28  1  0
  4 29  1  0
  4 30  1  0
  7 31  1  0
  8 32  1  0
  9 33  1  0
 11 34  1  0
 12 35  1  0
 13 36  1  0
 13 37  1  0
 14 38  1  0
 14 39  1  0
 15 40  1  0
 15 41  1  0
 16 42  1  0
 16 43  1  0
 17 44  1  0
 17 45  1  0
 17 46  1  0
 18 47  1  0
 18 48  1  0
 19 49  1  0
 19 50  1  0
 20 51  1  0
 20 52  1  0
 21 53  1  0
 21 54  1  0
 21 55  1  0
M  END

Similar Monomers

Structure
Similarity
IUPAC name
MF
Copolymers