Tert-butyl 3-hydroxy-4,4,8-trimethyl-5-oxo-7-(2,2,2-trichloroethoxycarbonyloxy)undec-10-enoate

An ester, C21H33Cl3O7, 503.847 g/mol.

Organic — ester

Identifiers

Molecular formula: C₂₁H₃₃Cl₃O₇
Molecular weight: 503.847 g/mol
Exact mass: 502.129186 g/mol
SMILES: C=CCC(C)C(CC(=O)C(C)(C)C(O)CC(=O)OC(C)(C)C)OC(=O)OCC(Cl)(Cl)Cl
InChI: InChI=1S/C21H33Cl3O7/c1-8-9-13(2)14(30-18(28)29-12-21(22,23)24)10-15(25)20(6,7)16(26)11-17(27)31-19(3,4)5/h8,13-14,16,26H,1,9-12H2,2-7H3
InChIKey: NZNZEWXNHGHEQH-UHFFFAOYSA-N

Open in ReactionLens Use in reaction prediction

Calculated properties

Derived from the structure, not from a sample; kept apart from the measurements above.

logP: 5.1687calculated · chemistry engine; Estimated preference for oil over water. Higher means more oil-like.
Topological polar surface area: 99.13 Å²calculated · chemistry engine; Surface area from polar atoms; relates to how easily a molecule crosses membranes.
H-bond donors: 1calculated · chemistry engine; Atoms that can donate a hydrogen bond.
H-bond acceptors: 7calculated · chemistry engine; Atoms that can accept a hydrogen bond.
Rotatable bonds: 11calculated · chemistry engine; Single bonds the molecule can freely twist around.
Molar refractivity: 120.3628 cm³/molcalculated · chemistry engine; Relates to the molecule's polarisability.
Fraction sp³ carbons: 0.7619calculated · chemistry engine; Share of carbon atoms with tetrahedral bonding.
QED drug-likeness: 0.2358calculated · chemistry engine; Quantitative estimate of drug-likeness (0–1).

What it is made of

Elements

C Carbon21 atoms · 50.1% by mass
O Oxygen7 atoms · 22.2% by mass
Cl Chlorine3 atoms · 21.1% by mass
H Hydrogen33 atoms · 6.6% by mass

Percentages are of the molecular weight above, worked out the same way the molar mass calculator does it.

Structure

Heavy atoms, hydrogen excluded: 31
Total atoms, hydrogen included: 64
Rings: 0
Aromatic rings: 0
Stereocentres: 3
Formal charge: 0

Functional groups

Ester
A carbonyl bonded to an oxygen that links to another carbon.
Ketone
A carbonyl bonded to two carbons.
Alcohol
An –OH group on a saturated carbon.
Ether
An oxygen bridging two carbons.
Halide (C–X)
A halogen atom attached to carbon.
Alkene
A carbon–carbon double bond.

Matched by structural pattern, not by a measurement.

The molecule in three dimensions

Rotate and inspect the atoms. Loaded only when you ask, so the page stays light.

The drawing above is a diagram of what is bonded to what. A molecule is not flat, and the model here is one low-energy shape generated from the connectivity — useful for seeing which groups can reach each other, and not a measured structure. A real sample is a population of conformations, interconverting.

Reactions it appears in

No documented reaction with a written procedure and a source involves Tert-butyl 3-hydroxy-4,4,8-trimethyl-5-oxo-7-(2,2,2-trichloroethoxycarbonyloxy)undec-10-enoate yet.

Structurally related

Nothing structurally close to Tert-butyl 3-hydroxy-4,4,8-trimethyl-5-oxo-7-(2,2,2-trichloroethoxycarbonyloxy)undec-10-enoate has a page here yet.

Where these values came from

chemistry engine
structure perception

No matching record was found in the currently indexed sources (reference compound database)..

What this page does not claim

Identifiers are copied from the source record, measured values are reported as published, and calculated values are marked as calculated. Nothing here is a hazard, purity or handling assessment — how the library is checked.