[2.2]Paracyclophane - CAS 1633-22-3
Catalog: |
BB011990 |
Product Name: |
[2.2]Paracyclophane |
CAS: |
1633-22-3 |
Synonyms: |
tricyclo[8.2.2.24,7]hexadeca-1(13),4,6,10(14),11,15-hexaene |
IUPAC Name: | tricyclo[8.2.2.24,7]hexadeca-1(13),4,6,10(14),11,15-hexaene |
Description: | [2.2]Paracyclophane (CAS# 1633-22-3) is a useful research chemical. |
Molecular Weight: | 208.30 |
Molecular Formula: | C16H16 |
Canonical SMILES: | C1CC2=CC=C(CCC3=CC=C1C=C3)C=C2 |
InChI: | InChI=1S/C16H16/c1-2-14-4-3-13(1)9-10-15-5-7-16(8-6-15)12-11-14/h1-8H,9-12H2 |
InChI Key: | OOLUVSIJOMLOCB-UHFFFAOYSA-N |
Boiling Point: | 320.7 °C at 760 mmHg |
Melting Point: | 285-288 °C |
Purity: | 95 % |
Density: | 1.033 g/cm3 |
Appearance: | Off-white. |
Storage: | Store in a cool, dry place. Keep container closed when not in use. |
MDL: | MFCD00003707 |
LogP: | 3.57040 |
GHS Hazard Statement: | H317 (100%): May cause an allergic skin reaction [Warning Sensitization, Skin] |
Precautionary Statement: | P260, P261, P272, P280, P302+P352, P314, P321, P333+P313, P363, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-113461628-A | Chiral thermal activation delayed fluorescence molecule based on [2.2] para-cyclophane and preparation method and application thereof | 20210716 |
CN-113149807-A | Triplet annihilator and preparation method and application thereof | 20210514 |
JP-2021056521-A | Mirror with image display function for vehicles | 20201204 |
CN-111689853-A | Layered bisphenol acrylate antioxidant and preparation method thereof | 20200628 |
JP-6823748-B1 | Coated article | 20200518 |
PMID | Publication Date | Title | Journal |
23046357 | 20121018 | Ab initio molecular orbital study on the excited states of [2.2]-, [3.3]-, and siloxane-bridged paracyclophanes | The journal of physical chemistry. A |
22847148 | 20120914 | A pass too far: dissociation of internal energy selected paracyclophane cations, theory and experiment | Physical chemistry chemical physics : PCCP |
22511277 | 20120814 | [2.2]Paracyclophane derived bisphosphines for the activation of hydrogen by FLPs: application in domino hydrosilylation/hydrogenation of enones | Dalton transactions (Cambridge, England : 2003) |
22800614 | 20120726 | How do strain and steric interactions affect the reactions of aromatic compounds with free radicals? Characterization of the radicals formed by muonium addition to p-xylene and [2.2]paracyclophane by DFT calculations and muon spin spectroscopy | The journal of physical chemistry. A |
22628138 | 20120702 | Theoretical approach towards the understanding of asymmetric additions of dialkylzinc to enals and iminals catalysed by [2.2]paracyclophane-based N,O-ligands | Chemistry (Weinheim an der Bergstrasse, Germany) |
Complexity: | 156 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 208.125200510 |
Formal Charge: | 0 |
Heavy Atom Count: | 16 |
Hydrogen Bond Acceptor Count: | 0 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 208.125200510 |
Rotatable Bond Count: | 0 |
Topological Polar Surface Area: | 0 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 3.7 |
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