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
1.8212 3.2781 2.9510 C 0 0 0 0 0 0 0 0 0 0 0 0
1.4856 3.6310 1.5347 C 0 0 0 0 0 0 0 0 0 0 0 0
0.4948 2.6394 0.8973 C 0 0 0 0 0 0 0 0 0 0 0 0
1.1597 1.2965 0.9184 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.0510 -0.2314 0.0326 Sn 0 0 0 0 0 4 0 0 0 0 0 0
-1.2006 -1.1859 1.5480 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.6767 -0.4711 2.6125 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.4488 -1.0536 3.6356 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.7237 -2.4115 3.5352 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.2644 -3.1557 2.4802 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.5067 -2.5206 1.5048 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.5430 -4.5823 2.3816 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.9713 -5.3510 3.2821 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.4146 0.5047 -1.3967 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.8171 0.8491 -2.7387 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.0314 1.3284 -3.5668 C 0 0 0 0 0 0 0 0 0 0 0 0
-1.6434 1.7261 -4.9578 C 0 0 0 0 0 0 0 0 0 0 0 0
1.2519 -1.6538 -0.8822 C 0 0 0 0 0 0 0 0 0 0 0 0
2.6437 -1.1787 -1.0754 C 0 0 0 0 0 0 0 0 0 0 0 0
2.8299 -0.0295 -2.0076 C 0 0 0 0 0 0 0 0 0 0 0 0
4.3032 0.3709 -2.0672 C 0 0 0 0 0 0 0 0 0 0 0 0
1.7235 4.1864 3.6169 H 0 0 0 0 0 0 0 0 0 0 0 0
2.8081 2.7902 3.0676 H 0 0 0 0 0 0 0 0 0 0 0 0
1.0317 2.5506 3.3017 H 0 0 0 0 0 0 0 0 0 0 0 0
1.0059 4.6222 1.5109 H 0 0 0 0 0 0 0 0 0 0 0 0
2.4184 3.6941 0.9032 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.3760 2.6028 1.6041 H 0 0 0 0 0 0 0 0 0 0 0 0
0.2089 2.9775 -0.1082 H 0 0 0 0 0 0 0 0 0 0 0 0
1.3020 1.0032 1.9952 H 0 0 0 0 0 0 0 0 0 0 0 0
2.1639 1.2615 0.4687 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.4910 0.5904 2.7150 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.8402 -0.5176 4.4691 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.3244 -2.8851 4.3124 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.1355 -3.1277 0.6685 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.3430 -5.0471 1.3564 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.2364 -5.1599 4.3398 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.1322 -6.4388 3.0642 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.0071 1.3714 -1.0223 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.1667 -0.3117 -1.5863 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.5088 -0.0857 -3.2536 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.0332 1.6044 -2.7152 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.5216 2.0993 -2.9640 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.7300 0.4415 -3.5790 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.0498 0.9808 -5.4891 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.2292 2.7522 -4.8943 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.6154 1.8590 -5.5348 H 0 0 0 0 0 0 0 0 0 0 0 0
1.2474 -2.5859 -0.2547 H 0 0 0 0 0 0 0 0 0 0 0 0
0.8755 -2.0014 -1.8861 H 0 0 0 0 0 0 0 0 0 0 0 0
3.2280 -2.0313 -1.5040 H 0 0 0 0 0 0 0 0 0 0 0 0
3.1488 -0.9466 -0.0942 H 0 0 0 0 0 0 0 0 0 0 0 0
2.6213 -0.3484 -3.0829 H 0 0 0 0 0 0 0 0 0 0 0 0
2.2490 0.8720 -1.8068 H 0 0 0 0 0 0 0 0 0 0 0 0
4.8870 -0.4976 -2.3943 H 0 0 0 0 0 0 0 0 0 0 0 0
4.4625 1.1931 -2.7882 H 0 0 0 0 0 0 0 0 0 0 0 0
4.6615 0.7330 -1.0576 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