Basic information
- CAS
139136-72-4- Standard SMILES
CCCCCCCC1CCC(c2ccc(F)c(F)c2)CC1- InChIKey
XZJQPRYOMYTPOL-UHFFFAOYSA-N- Molecular formula
- C19H28F2
- Average molar mass
- 294.4 g/mol
- Monoisotopic mass
- 294.21590722
Names & identifiers
- Preferred name
- 1,2-Difluoro-4-(4-heptylcyclohexyl)benzene
- IUPAC
- 1,2-difluoro-4-(4-heptylcyclohexyl)benzene
- English name
- TRANS-4''-HEPTYLCYCLOHEXYL-3,4-DIFLUOROBENZENE
- Molecular formula
- C19H28F2
- Molecular weight
- 294.42
Names & synonyms
139136-72-41,2-Difluoro-4-(4-heptylcyclohexyl)benzeneDTXSID60343147RefChem:215931DTXCID202942271,2-Difluoro-4-((1s,4r)-4-heptylcyclohexyl)benzeneTRANS-4/'/'-HEPTYLCYCLOHEXYL-3,4-DIFLUOROBENZENE7cHdFPSCHEMBL7514095SCHEMBL7572804TRANS-1,2-DIFLUORO-4-(4-HEPTYL-CYCLOHEXYL)-BENZENEDB-299307
Show more names
7-HB(F)-FHeptylcyclohexyl-3,4-difluorobenzeneTRANS-4''-HEPTYLCYCLOHEXYL-3,4-DIFLUOROBENZENEBenzene, 1,2-difluoro-4-(trans-4-heptylcyclohexyl)-
1,2-Difluoro-4-(4-heptylcyclohexyl)benzene #Benzene, 1,2-difluoro-4-(4-heptylcyclohexyl)-1,2-Difluoro-4-(trans-4-heptylcyclohexyl)benzene
Database identifiers
- CAS
139136-72-4- PubChem CID
- 587773
- DTXSID
DTXSID60343147
Properties
Computed structural properties
- XLogP
- 8.2
- Topological polar surface area
- 0 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 2
- Rotatable bonds
- 7
- Heavy atoms
- 21
- Formal charge
- 0
- Complexity
- 271
Experimental & physicochemical properties
Chemical Classes
Fluorinated Liquid Crystal Monomers (LCM)
Liquid Crystal (LCM) Monomers
Physicochemical properties
- Boiling point
- 353.235 · 353.235±35.00 °C(Press: 760.00 Torr)(predicted)
- Density
- 0.984 · 0.984±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
Chemistry & industry
Suppliers5 total
湖北魏氏化学试剂股份有限公司13125137732 18686406941 · [email protected]
Alchem Pharmtech,Inc.8485655694 · [email protected]
湖北魏氏化学试剂股份有限公司027-59102966 18717199209 · [email protected]
山东彬睿特新材料有限公司0533-2866658 15615638350 · [email protected]
烟台丰蓬液晶材料有限公司18754503080 · [email protected]
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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