(R)-(+)-2-Hydroxy-1,2,2-triphenylethyl Acetate - CAS 95061-47-5
Catalog: |
BB041604 |
Product Name: |
(R)-(+)-2-Hydroxy-1,2,2-triphenylethyl Acetate |
CAS: |
95061-47-5 |
Synonyms: |
acetic acid [(1R)-2-hydroxy-1,2,2-triphenylethyl] ester; [(1R)-2-hydroxy-1,2,2-triphenylethyl] acetate |
IUPAC Name: | [(1R)-2-hydroxy-1,2,2-triphenylethyl] acetate |
Description: | (R)-(+)-2-Hydroxy-1,2,2-triphenylethyl Acetate (CAS# 95061-47-5) is a useful research chemical. |
Molecular Weight: | 332.39 |
Molecular Formula: | C22H20O3 |
Canonical SMILES: | CC(=O)OC(C1=CC=CC=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)O |
InChI: | InChI=1S/C22H20O3/c1-17(23)25-21(18-11-5-2-6-12-18)22(24,19-13-7-3-8-14-19)20-15-9-4-10-16-20/h2-16,21,24H,1H3/t21-/m1/s1 |
InChI Key: | GXLZCXZLVDUDHP-OAQYLSRUSA-N |
Boiling Point: | 487.6 °C at 760 mmHg |
Density: | 1.18 g/cm3 |
Storage: | Sealed in dry, Room Temperature |
MDL: | MFCD00066242 |
LogP: | 4.22690 |
Publication Number | Title | Priority Date |
WO-2021076238-A1 | Clear nail top coat compositions and methods of making | 20191017 |
CZ-20003451-A3 | Novel cephalotaxane derivatives and process of their preparation | 19990317 |
US-2002010339-A1 | Method for synthesis of halopyridyl-acyclopentane derivative and intermediate thereof | 19980526 |
US-6384228-B2 | Method for synthesis of halopyridyl-azacyclopentane derivative and intermediate thereof | 19980526 |
AU-3270699-A | Novel cephalotaxane derivatives and process for their preparation | 19980320 |
Complexity: | 397 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 1 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 332.1412445 |
Formal Charge: | 0 |
Heavy Atom Count: | 25 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 332.1412445 |
Rotatable Bond Count: | 6 |
Topological Polar Surface Area: | 46.5 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 4 |
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