| Weight | 104.152 g/mol |
|---|---|
| Formula | C8H8 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
Bicyclo[4.2.0]octa-1,3,5-triene (694-87-1)
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- Photolysis of Bicyclo[4,2,0]octa-2,4-diene, Cycloocta-1,3,5-triene and Cycloocta-1,3,6-triene (Angewandte Chemie, 1964)
- Bicyclo[4.2.0]octa1,3,5triene: 2Mono and 2,5Disubstituted Derivatives via Highly Regioselective Lithiation of Its Cr(CO)3 Complex and via Reductive Silylation/Oxidation (Helvetica Chimica Acta, 1990)
- The photolysis of exo-1,6-dimethyl-7,8-diphenyl tricyclo [4.2.1.02,5]nona-3,7-dien-9-one. Part 1. Isolation and characterisation of a stable bicyclo[4.2.0]octa-2,4,7-triene (Tetrahedron Letters, 1970)
- Trapping of 1,3,5,7-cyclooctatetraene valence tautomers. Thermodynamic stability of bicyclo[4.2.0]octa-2,4,7-triene (Journal of Organic Chemistry, 1986)
- Heats of Formation of 1,3,5,7-Cyclooctatetraene and Bicyclo[4.2.0]octa-2,4,7-triene. A High-Level ab Initio Study (Journal of Physical Chemistry A, 1998)
- Structure of 3,4-bis(trimethylsilyl)bicyclo[4.2.0]octa-1,3,5-triene (Acta Crystallographica Section B Structural Crystallography and Crystal Chemistry, 1981)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CC2=CC=CC=C21
-
InChIKeyUMIVXZPTRXBADB-UHFFFAOYSA-N
- Pubchem - Bicyclo[4.2.0]octa-1,3,5-triene
- Wikipedia - benzocyclobutene
Benzocyclobutene (BCB) is a benzene ring fused to a cyclobutane ring. It has chemical formula C8H8. BCB is frequently used to create photosensitive polymers.
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Bicyclo[4.2.0]octa-1,3,5-triene
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