(±)-trans-1,3-Diphenylallyl acetate - CAS 87751-69-7
Catalog: |
BB038623 |
Product Name: |
(±)-trans-1,3-Diphenylallyl acetate |
CAS: |
87751-69-7 |
Synonyms: |
0 |
IUPAC Name: | [(E)-1,3-diphenylprop-2-enyl] acetate |
Description: | (±)-trans-1,3-Diphenylallyl acetate (CAS# 87751-69-7 ) is a useful research chemical. |
Molecular Weight: | 252.31 |
Molecular Formula: | C17H16O2 |
Canonical SMILES: | 0 |
InChI: | 0 |
InChI Key: | 0 |
LogP: | 4.00420 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
WO-2020033567-A1 | Methods and compositions for substituted arylcycloheptane analogs | 20180807 |
US-2021300928-A1 | Methods and compositions for substituted arylcycloheptane analogs | 20180807 |
CN-111868065-A | C-sterically hindered P-chirally derived organophosphorus compounds | 20180320 |
US-2020407381-A1 | C-bulky p-chirogenic organophosphorus compounds | 20180320 |
US-10565015-B2 | Spiroketal-based C2-symmetric scaffold for asymmetric catalysis | 20170918 |
PMID | Publication Date | Title | Journal |
21964571 | 20111128 | Chiral phosphinoferrocene carboxamides with amino acid substituents as ligands for Pd-catalysed asymmetric allylic substitutions. Synthesis and structural characterisation of catalytically relevant Pd complexes | Dalton transactions (Cambridge, England : 2003) |
20949947 | 20110118 | Artificial metalloenzymes based on the biotin-avidin technology: enantioselective catalysis and beyond | Accounts of chemical research |
20863121 | 20101015 | Chiral phosphaalkene-oxazoline ligands for the palladium-catalyzed asymmetric allylic alkylation | Organic letters |
20803749 | 20101001 | (S)-6-Bromo-BINOL-based phosphoramidite ligand with C(1) symmetry for enantioselective hydrogenation and allylic substitution | Chirality |
20930416 | 20101001 | Sterically congested, 'roofed' β-iminodisulfides as new chiral ligands for palladium-catalyzed, asymmetric allylic alkylation | Chemical & pharmaceutical bulletin |
Complexity: | 296 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 1 |
Exact Mass: | 252.115029749 |
Formal Charge: | 0 |
Heavy Atom Count: | 19 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 252.115029749 |
Rotatable Bond Count: | 5 |
Topological Polar Surface Area: | 26.3 Å2 |
Undefined Atom Stereocenter Count: | 1 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 3.9 |
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