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Thermo Scientific Chemicals
1,3-Cyclohexadiene, 96%, stab. with 0.1% BHT
CAS: 592-57-4 | C6H8 | 80.13 g/mol
化学物質識別子
CAS592-57-4
IUPAC Namecyclohexa-1,3-diene
Molecular FormulaC6H8
InChI KeyMGNZXYYWBUKAII-UHFFFAOYSA-N
SMILESC1CC=CC=C1
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)Clear colorless
Refractive Index1.4715-1.4765 @ 20*C
Stabilizer0.1% BHT
FormLiquid
Assay (GC)≥95.0%
1,3-Cyclohexadiene is used as a hydrogen donor in transfer hydrogenation. It is used in the conversion to benzene. It is useful in the study of proteomics research.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
1,3-Cyclohexadiene is used as a hydrogen donor in transfer hydrogenation. It is used in the conversion to benzene. It is useful in the study of proteomics research.
Solubility
Slightly miscible with methanol. Immiscible with water.
Notes
Incompatible with strong oxidizing agents. Store in a cool place.
1,3-Cyclohexadiene is used as a hydrogen donor in transfer hydrogenation. It is used in the conversion to benzene. It is useful in the study of proteomics research.
Solubility
Slightly miscible with methanol. Immiscible with water.
Notes
Incompatible with strong oxidizing agents. Store in a cool place.
RUO – Research Use Only
General References:
- Ohta, A.; Kobayashi, O.; Danielache, S. O.; Nanbu, S. Nonadiabatic ab initio molecular dynamics of photoisomerization reaction between 1, 3-cyclohexadiene and 1, 3, 5-cis-hexatriene. Chem. Phys. 2015, 459, 45-53.
- Adachi, S.; Sato, M.; Suzuki, T. Direct Observation of Ground-State Product Formation in a 1,3-Cyclohexadiene Ring-Opening Reaction. J. Phys. Chem. Lett. 2015, 6 (3), 343-346.