RHODINYL FORMATE
Relevant Data
Food Additives Approved by WHO:
Flavouring Substances Approved by European Union:
General Information
| Mainterm | RHODINYL FORMATE |
| Doc Type | ASP |
| CAS Reg.No.(or other ID) | 141-09-3 |
| Regnum |
172.515 |
From www.fda.gov
Computed Descriptors
Download SDF| 2D Structure | |
| CID | 61092 |
| IUPAC Name | 3,7-dimethyloct-7-enyl formate |
| InChI | InChI=1S/C11H20O2/c1-10(2)5-4-6-11(3)7-8-13-9-12/h9,11H,1,4-8H2,2-3H3 |
| InChI Key | VMBKZHMLQXCNCP-UHFFFAOYSA-N |
| Canonical SMILES | CC(CCCC(=C)C)CCOC=O |
| Molecular Formula | C11H20O2 |
| Wikipedia | rhodinyl formate |
From Pubchem
Computed Properties
| Property Name | Property Value |
|---|---|
| Molecular Weight | 184.279 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 8 |
| Complexity | 152.0 |
| CACTVS Substructure Key Fingerprint | A A A D c e B w M A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A G g A A A A A A D Q C g g A M C C A A A B A C I A g B C i A A A A A A g A A A A A A A A A A g A A A I A A Q A A A A A E g A A A A A G A w O A O A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A = = |
| Topological Polar Surface Area | 26.3 |
| Monoisotopic Mass | 184.146 |
| Exact Mass | 184.146 |
| XLogP3 | None |
| XLogP3-AA | 4.1 |
| Compound Is Canonicalized | True |
| Formal Charge | 0 |
| Heavy Atom Count | 13 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Isotope Atom Count | 0 |
| Covalently-Bonded Unit Count | 1 |
From Pubchem
ADMET Predicted Profile --- Classification
| Model | Result | Probability |
|---|---|---|
| Absorption | ||
| Blood-Brain Barrier | BBB+ | 0.9627 |
| Human Intestinal Absorption | HIA+ | 0.9767 |
| Caco-2 Permeability | Caco2+ | 0.7250 |
| P-glycoprotein Substrate | Non-substrate | 0.6439 |
| P-glycoprotein Inhibitor | Non-inhibitor | 0.7373 |
| Non-inhibitor | 0.7949 | |
| Renal Organic Cation Transporter | Non-inhibitor | 0.8045 |
| Distribution | ||
| Subcellular localization | Mitochondria | 0.5829 |
| Metabolism | ||
| CYP450 2C9 Substrate | Non-substrate | 0.8929 |
| CYP450 2D6 Substrate | Non-substrate | 0.8794 |
| CYP450 3A4 Substrate | Non-substrate | 0.5374 |
| CYP450 1A2 Inhibitor | Non-inhibitor | 0.6481 |
| CYP450 2C9 Inhibitor | Non-inhibitor | 0.9335 |
| CYP450 2D6 Inhibitor | Non-inhibitor | 0.9391 |
| CYP450 2C19 Inhibitor | Non-inhibitor | 0.9051 |
| CYP450 3A4 Inhibitor | Non-inhibitor | 0.8766 |
| CYP Inhibitory Promiscuity | Low CYP Inhibitory Promiscuity | 0.7857 |
| Excretion | ||
| Toxicity | ||
| Human Ether-a-go-go-Related Gene Inhibition | Weak inhibitor | 0.8394 |
| Non-inhibitor | 0.8840 | |
| AMES Toxicity | Non AMES toxic | 0.9284 |
| Carcinogens | Non-carcinogens | 0.5386 |
| Fish Toxicity | High FHMT | 0.9720 |
| Tetrahymena Pyriformis Toxicity | High TPT | 0.9813 |
| Honey Bee Toxicity | High HBT | 0.8188 |
| Biodegradation | Ready biodegradable | 0.9683 |
| Acute Oral Toxicity | III | 0.6552 |
| Carcinogenicity (Three-class) | Non-required | 0.5862 |
From admetSAR
ADMET Predicted Profile --- Regression
| Model | Value | Unit |
|---|---|---|
| Absorption | ||
| Aqueous solubility | -3.2560 | LogS |
| Caco-2 Permeability | 1.2017 | LogPapp, cm/s |
| Distribution | ||
| Metabolism | ||
| Excretion | ||
| Toxicity | ||
| Rat Acute Toxicity | 1.4365 | LD50, mol/kg |
| Fish Toxicity | -0.1622 | pLC50, mg/L |
| Tetrahymena Pyriformis Toxicity | 0.7605 | pIGC50, ug/L |
From admetSAR
Taxonomic Classification
| Kingdom | Organic compounds |
|---|---|
| Superclass | Lipids and lipid-like molecules |
| Class | Fatty Acyls |
| Subclass | Fatty alcohol esters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Fatty alcohol esters |
| Alternative Parents | |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Fatty alcohol ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Description | This compound belongs to the class of organic compounds known as fatty alcohol esters. These are ester derivatives of a fatty alcohol. |
From ClassyFire