| Common Name |
(Acetyloxy)triphenylstannane
| Description |
Nonsystemic fungicide(Acetyloxy)triphenylstannane belongs to the family of Aromatic Homomonocyclic Compounds. These are aromatic compounds containig only one ring, which is homocyclic.
| Structure |
MOLSDFPDBSMILESInChI
Structure for HMDB31789 ((Acetyloxy)triphenylstannane)
| Synonyms |
| Value |
Source |
AcetatotriphenylstannaneChEBI
Acetic acid, triphenylstannyl esterChEBI
Acetoxy-triphenyl-stannanChEBI
AcetoxytriphenylstannaneChEBI
AcetoxytriphenyltinChEBI
Fentin azetatChEBI
Phentin acetateChEBI
PhentinoacetateChEBI
Tin triphenyl acetateChEBI
Triphenyl-zinnacetatChEBI
triphenylaceto StannaneChEBI
Triphenylstannium acetateChEBI
Triphenylstannyl acetateChEBI
Triphenyltin acetateChEBI
Triphenyltin(IV) acetateChEBI
Acetate, triphenylstannyl esterGenerator
Phentin acetic acidGenerator
Phentinoacetic acidGenerator
Tin triphenyl acetic acidGenerator
Triphenylstannium acetic acidGenerator
Triphenylstannyl acetic acidGenerator
Triphenyltin acetic acidGenerator
Triphenyltin(IV) acetic acidGenerator
(Acetyloxy)(triphenyl)stannaneHMDB
(Acetyloxy)triphenyl-stannaneHMDB
Acetate de triphenyl-etainHMDB
acetato Di stagno trifenileHMDB
Acetoxy-triphenylstannaneHMDB
Acetoxytriphenyl-stannaneHMDB
Acetoxytriphenyl-tinHMDB
BatasanHMDB
Benzaldehyde, m-nitro-, 3-thio-4-O-tolylsemicarbazoneHMDB
BrestanHMDB
Brestan 60HMDB
fenolovo AcetateHMDB
Fentin acetaatHMDB
Fentin acetatHMDB
Fentin acetateHMDB
FentinacetatHMDB
Fentine acetateHMDB
Fintin acetatoHMDB
LiromatinHMDB
LirostanolHMDB
m-Nitrobenzaldehyde 3-thio-4-O-tolylsemicarbazoneHMDB
Phenostat aHMDB
SUZUHMDB
TinestanHMDB
Tinestan 60 WPHMDB
Tinestan WP 20HMDB
Tinestan WP 60HMDB
TPTAHMDB
TPZAHMDB
Trifenil stagno acetatoHMDB
Trifenyl-tinacetaatHMDB
| Chemical Formlia |
C20H18O2Sn
| Average Molecliar Weight |
409.07
| Monoisotopic Molecliar Weight |
410.032876391
| IUPAC Name |
triphenylstannyl acetate
| Traditional Name |
batasan
| CAS Registry Number |
900-95-8
| SMILES |
CC(=O)O[Sn](C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
| InChI Identifier |
InChI=1S/3C6H5.C2H4O2.Sn/c3*1-2-4-6-5-3-1;1-2(3)4;/h3*1-5H;1H3,(H,3,4);/q;;;;+1/p-1
| InChI Key |
WDQNIWFZKXZFAY-UHFFFAOYSA-M
| Chemical Taxonomy |
| Description |
This compound belongs to the class of chemical entities known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
| Kingdom |
Chemical entities
| Super Class |
Organic compounds
| Class |
Benzenoids
| Sub Class |
Benzene and substituted derivatives
| Direct Parent |
Benzene and substituted derivatives
| Alternative Parents |
Metal aryls
Monocarboxylic acids and derivatives
Carboxylic acids
Organotin compounds
Organic salts
Organic oxides
Hydrocarbon derivatives
Carbonyl compounds
| Substituents |
Metal aryl
Monocyclic benzene moiety
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organic salt
Organotin compound
Organooxygen compound
Organometallic compound
Organic post-transition metal moeity
Carbonyl group
Aromatic homomonocyclic compound
| Molecliar Framework |
Not Available
| External Descriptors |
acetate ester (CHEBI:81918 )
organotin compound (CHEBI:81918 )
Organotin fungicides (C18728 )
| Ontology |
| Status |
Expected but not Quantified
| Origin |
Endogenous
Food
| Biofunction |
Not Available
| Application |
Agriclitural Chemical
| Cellliar locations |
Membrane
| Physical Properties |
| State |
Not Available
| Experimental Properties |
| Property |
Value |
Reference |
Melting Point121 – 123 °CNot Available
Boiling PointNot AvailableNot Available
Water Solubility0.009 mg/mL at 20 °CNot Available
LogPNot AvailableNot Available
| Predicted Properties |
| Property |
Value |
Source |
Water Solubility0.0028 mg/mLALOGPS
logP5.38ALOGPS
logP3.09ChemAxon
logS-5.2ALOGPS
pKa (Strongest Basic)-6.7ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count1ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area26.3 Å2ChemAxon
Rotatable Bond Count5ChemAxon
Refractivity88.14 m3·mol-1ChemAxon
Polarizability35.12 Å3ChemAxon
Number of Rings3ChemAxon
Bioavailability1ChemAxon
Rlie of FiveYesChemAxon
Ghose FilterYesChemAxon
Vebers RlieYesChemAxon
MDDR-like RlieYesChemAxon
| Spectra |
| Spectra |
Not Available
| Biological Properties |
| Cellliar Locations |
Membrane
| Biofluid Locations |
Not Available
| Tissue Location |
Not Available
| Pathways |
Not Available
| Normal Concentrations |
| Not Available |
| Abnormal Concentrations |
|
Not Available
| Associated Disorders and Diseases |
| Disease References |
None
| Associated OMIM IDs |
None
| External Links |
| DrugBank ID |
Not Available
| DrugBank Metabolite ID |
Not Available
| Phenol Explorer Compound ID |
Not Available
| Phenol Explorer Metabolite ID |
Not Available
| FoodDB ID |
FDB008462
| KNApSAcK ID |
Not Available
| Chemspider ID |
8085060
| KEGG Compound ID |
C18728
| BioCyc ID |
Not Available
| BiGG ID |
Not Available
| Wikipedia Link |
Not Available
| NuGOwiki Link |
HMDB31789
| Metagene Link |
HMDB31789
| METLIN ID |
Not Available
| PubChem Compound |
16682804
| PDB ID |
Not Available
| ChEBI ID |
Not Available
Product: MMAD (hydrochloride)
References |
| Synthesis Reference |
Not Available |
| Material Safety Data Sheet (MSDS) |
Not Available |
| General References |
- (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
|
PMID: 15180479