acetofenone
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composto chimico
Risorse esterne
| CSD Refcode | |
| numero ZVG | |
| HCIS ID | |
| identificativo DSSTOX di un composto chimico | |
| identificativo ChEMBL | |
| identificativo Gran Enciclopèdia Catalana | |
| identificativo ICSC | |
| Römpp online ID | |
| identificativo Grande Enciclopedia Russa | |
| identificativo ECHA InfoCard | |
| UM-BBD compound ID | |
| identificativo PDB | |
| CAMEO Chemicals ID | |
| CCDC Number | |
| identificativo della Enciclopedia della Cina (terza edizione) | |
| identificativo J9U della Biblioteca nazionale israeliana | |
| identificativo Freebase | |
| identificativo Microsoft Academic | |
| identificativo della Biblioteca del Congresso | |
| identificativo PubChem | |
| identificativo composto UniChem | |
| identificativo UNII | |
| identificativo PDB ligando | |
| SPLASH | |
| PesticideInfo chemical ID | |
| identificativo ChEBI | |
| identificativo DSSTOX sostanza | |
| identificativo OpenAlex | |
| Cannabis Database ID | |
| identificativo Gran Enciclopèdia Catalana (obsoleto) | |
| identificativo Thesaurus BNCF | |
| InChIKey | |
| identificativo ScienceDirect di un argomento | |
| identificativo Elhuyar ZTH | |
| numero CosIng | |
| identificativo HMDB | |
| SureChEMBL ID | |
| identificativo Store norske leksikon | |
| identificativo Den Store Danske | |
| InChI | |
| identificativo MeSH | |
| AICS Chemical ID (BEING DELETED) | |
| FL number | 07.004[21] |
| identificativo KNApSAcK | |
| numero CAS | |
| JECFA number | 806[24] |
| Probes And Drugs ID | |
| OSHA Occupational Chemical Database ID | |
| identificativo ChemSpider | |
| numero CE | 202-708-7[11] |
| identificativo GND | |
| MassBank accession ID | |
| identificativo KEGG | |
| Great Russian Encyclopedia portal ID | |
| identificativo Drugbank | |
| NSC number | |
| identificativo HSDB |
no tipo 'e
type of chemical entity
sottoclasse di
composto chimico
struttura chimica
massa
120,058 unità e' massa atomeca[28]
formula chimica
C₈H₈O[9]
SMILES canonico
CC(=O)C1=CC=CC=C1[9]
energia di ionizzazione
momento di dipolo elettrico
massa volumica
punto di fusione
punto di ebollizione
202,1±0,2 grado Celsius[31]
pressione: 101,325 kilopascal
uncertainty corresponds to: expanded uncertainty
punti di fase
punto critico[32]
pressione: 4,01±0,05 megapascal
volume molare: 373±40 centimetro cubo per mole
temperatura: 709,5±0,7 kelvin
viscosità dinamica
1,681 millipascal second[33]
fase della materia: liquido
temperatura: 25 grado Celsius
pressione: 1 atmosfera
0,634 millipascal second[33]
fase della materia: liquido
temperatura: 100 grado Celsius
pressione: 1 atmosfera
tensione di superficie
pressione di vapore
solubilità
indice di rifrazione
sistema cristallino
sistema monoclino[31]
punto di infiammabilità
lower flammable limit
55 gram per cubic metre[35]
classificazione ed etichettatura di sicurezza
NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response[39]
NFPA salute: 2
NFPA speciali: nisciuno valore
NFPA infiammabilità: 2
NFPA reattività: 0
regolamento CLP[40]
GHS hazard pictogram: GHS07: punto esclamativo
GHS hazard statement: H302, H319
GHS precautionary statement: P305+P351+P338
parola di segnalazione GHS: danger
trovato nella tassonomia de
Opuntia ficus-indica[43]
rooibos[44]
Paeonia lactiflora[45]
dahpne odora[46]
Averrhoa carambola[47]
Hypericum hyssopifolium[48]
Nepeta racemosa[51]
Amorphophallus cicatricifer[52]
Aronia melanocarpa[53]
Artemisia xanthochroa[54]
Basella alba[55]
Bellis perennis[56]
Castanopsis cuspidata[57]
Chamaecrista greggii[58]
Euphorbia cyparissias[60]
Evernia prunastri[61]
Gossypium hirsutum[62]
Helichrysum ambiguum[63]
Malpighia punicifolia[64]
Nepeta nepetella[65]
Ophrys sphegodes[66]
Polygala senega[67]
Sauromatum venosum[68]
Scutellaria baicalensis[69]
Strobilanthes auriculatus[70]
Syzygium aromaticum[71]
Tamarix aphylla[72]
Trifolium pratense[74]
Medicago sativa[75]
Vaccinium macrocarpon[76]
Baccharis[77]
Acca sellowiana[78]
Strobilanthes auriculata[70]
Elsholtzia eriostachya[79]
mango[80]
Cymbopogon citratus[81]
Malpighia glabra[64]
Malpighia emarginata[64]
Chrysocephalum ambiguum[63]
Tricholoma matsutake[85]
descritto nella fonte
Grande Enciclopedia Sovietica (1926-1947)
dichiarazione è argomento di: Q43447952
Encyclopædia Britannica (1911)
dichiarazione è argomento di: 1911 Encyclopædia Britannica/Acetophenone
Meyers Konversations-Lexikon (1888–1889)
dichiarazione è argomento di: Q112753740
Grande Enciclopedia Sovietica (1926-1947)
dichiarazione è argomento di: Q110375593
caratterizzato da
amaro[86]
MCN code
2914.39.10
è fatte 'e
ossigeno
carbonio
categoria su Commons
Acetophenone
Riferimento
- ↑ 1,0 1,1 Cambridge Structural Database, 10 Jen 2023, InChIKey match
- ↑ 2,0 2,1 ChEMBL, 20 Nuv 2016, Lengua ngrese, ACETOPHENONE, CHEMBL274467
- ↑ ECHA Substance Infocard database, 27 dic 2018, 100.002.462, Acetophenone, CAS no.: 98-86-2
- ↑ Protein Data Bank, 19 ott 2016, Lengua ngrese, 1ZK4, 1ZK4
- ↑ Protein Data Bank, 19 ott 2016, Lengua ngrese, 1ZK1, 1ZK1
- ↑ National Library of Israel Names and Subjects Authority File
- ↑ Freebase Data Dumps, 28 ott 2013
- ↑ Gemeinsame Normdatei
- ↑ 9,0 9,1 9,2 9,3 9,4 PubChem, 20 Nuv 2016, Lengua ngrese, 7410, ACETOPHENONE
- ↑ UniChem
- ↑ 11,0 11,1 11,2 Global Substance Registration System, 20 Nuv 2016, Lengua ngrese, acetophenone, RK493WHV10
- ↑ 12,0 12,1 12,2 12,3 KWOLFJPFCHCOCG-UHFFFAOYSA-N, InChIKey
- ↑ Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
- ↑ OpenAlex, 26 Jen 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
- ↑ Cannabis Database
- ↑ Biblioteca Nazionale Centrale di Firenze
- ↑ ChEBI release 2020-09-01
- ↑ CosIng database, 28 dic 2019, 74153, ACETOPHENONE, CAS no.: 98-86-2
- ↑ 19,0 19,1 19,2 inferred from InChIKey
- ↑ Medical Subject Headings, 14 Màr 2018, C038699
- ↑ EFSA database, 23 Jen 2021, CAS no.: 98-86-2, 07.004
- ↑ ChEBI, 19 ott 2016, Lengua ngrese, acetophenone, 27632
- ↑ CAS Common Chemistry, 8 Abb 2021, KWOLFJPFCHCOCG-UHFFFAOYSA-N, https://commonchemistry.cas.org/detail?cas_rn=98-86-2
- ↑ Evaluations of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 13 Maj 2021
- ↑ ChemSpider, 20 Nuv 2016, Lengua ngrese, 7132, Acetophenone
- ↑ DrugBank, 20 Nuv 2016, Lengua ngrese, 04619, ACETOPHENONE
- ↑ Hazardous Substances Data Bank, 10 Maj 2021, 28 ott 2019, Acetophenone, 969
- ↑ PubChem, 19 ott 2016, Lengua ngrese, 7410, ACETOPHENONE
- ↑ Basic laboratory and industrial chemicals: A CRC quick reference handbook
- ↑ CRC Handbook of Chemistry and Physics (97th edition), 9-60
- ↑ 31,0 31,1 31,2 31,3 31,4 CRC Handbook of Chemistry and Physics (97th edition), 3-6
- ↑ CRC Handbook of Chemistry and Physics (97th edition), 6-67
- ↑ 33,0 33,1 CRC Handbook of Chemistry and Physics (97th edition), 6-243
- ↑ 34,0 34,1 34,2 CRC Handbook of Chemistry and Physics (97th edition), 6-190
- ↑ 35,0 35,1 35,2 35,3 35,4 35,5 35,6 35,7 database GESTIS, 30 lug 2018, Lengua ngrese, 22380, Acetophenone
- ↑ 36,0 36,1 36,2 CRC Handbook of Chemistry and Physics (97th edition), 15-13, 16-17
- ↑ 37,0 37,1 37,2 CRC Handbook of Chemistry and Physics (97th edition), 5-139
- ↑ CRC Handbook of Chemistry and Physics (97th edition), 5-173
- ↑ 30 lug 2018, Fisher Scientific, Lengua ngrese, https://fscimage.fishersci.com/msds/00002.htm, Acetophenone, 99%, 10 dic 2007
- ↑ database GESTIS, 30 lug 2018, Lengua ngrese, 22380, Acetophenone, 2016
- ↑ Studies on the Volatile Compounds of Camellia Flowers
- ↑ Volatile Compounds from Flowers
- ↑ Volatile constituents of prickly pear (Opuntia ficus indica Mill., de Castilla variety)
- ↑ Volatile components of Rooibos tea (Aspalathus linearis)
- ↑ "Essential oil constituents of \"PAEONIAE RADIX\" Peaonia lactiflora Pall. (P. albilora Pall.)."
- ↑ Volatile components of zinchoge flower (Daphne odora Thunb.).
- ↑ Volatile constituents of carambola (Averrhoa carambola L.)
- ↑ Composition and antifungal activity of essential oils isolated fromHypericum hyssopifolium andHypericum heterophyllum
- ↑ Terpenoids from Elsholtzia Species; II1. Constituents of Essential Oil from a New Chemotype of Elsholtzia cristata
- ↑ Composition of the Essential Oils from the Aerial Parts ofElsholtzia ciliata(Thunb.) Hyland. from Vietnam
- ↑ Composition of the Essential Oil of Nepeta racemosa Lam.
- ↑ Inflorescence odours of Amorphophallus and Pseudodracontium (Araceae)
- ↑ Analysis of the volatile constituents of black chokeberry (Aronia melanocarpa Ell.)
- ↑ Prenylated coumarates from Artemisia xanthochroa
- ↑ Volatile flavor components of malabar-nightshade (Basella rubra L.)
- ↑ Acetylenes and terpenoids of Bellis perennis
- ↑ Volatile constituents of Castanopsis flower
- ↑ Cassanes and anthraquinones from Chamaecrista greggii
- ↑ Volatile flavor components of watermelon (Citrullus vulgaris).
- ↑ Biologically Active Compounds from the Euphorbiaceae; 2. Two Triterpenoids ofEuphorbia cyparissias
- ↑ Qualitative analysis of the odoriferous fraction of oakmoss (Evernia prunastri)
- ↑ Survey of the volatile constituents of cotton lint and waste with regard to byssinosis
- ↑ 63,0 63,1 Composition and antibacterial activity of the essential oils of Helichrysum rupestre and H. ambiguum growing in the Balearic Islands (Part III)
- ↑ 64,0 64,1 64,2 Chemical composition of acerola fruit (Malpighia punicifolia L.) at three stages of maturity
- ↑ Constituents of Essential Oil of Nepeta nepetella
- ↑ Volatiles from the flowers of four species in the sections arachnitiformes and araneiferae of the genus Ophrys as insect mimetic attractants
- ↑ Volatile compounds ofPolygala senega L. var.latifolia Torrey et Gray roots
- ↑ Dimethyl oligosulphides, major volatiles released from Sauromatum guttatum and Phallus impudicus
- ↑ Essential oil of Scutellaria baicalensis G.
- ↑ 70,0 70,1 Constituents of the Essential Oil ofStrobilanthes auriculatus
- ↑ Volatile components of clove essential oil (Eugenia caryophyllus SPRENG): Neutral fraction.
- ↑ Antimicrobial Activity and Phytochemical Constituents of Leaf Extracts of Cassia auriculata
- ↑ Steam volatile aroma constituents of roasted cocoa beans
- ↑ Volatile components of red clover leaves, flowers, and seed pods: possible insect attractants
- ↑ Volatiles from Medicago sativa complex flowers
- ↑ The Aroma of Cranberries. II. Vaccinium macrocarpon Ait.
- ↑ Plant growth inhibitory activity of p-hydroxyacetophenones and tremetones from Chilean endemic Baccharis species and some analogous: a comparative study
- ↑ Compositional Analysis and Aroma Evaluation of Feijoa Essential Oils from New Zealand Grown Cultivars
- ↑ The Essential Oil fromElsholtzia eriostachyavar.pusilla
- ↑ Volatile components from mango (Mangifera indica L.) cultivars
- ↑ GC-MS evaluation of Cymbopogon citratus (DC) Stapf oil obtained using modified hydrodistillation and microwave extraction methods
- ↑ Comparison of different extraction methods: steam distillation, simultaneous distillation and extraction and headspace co-distillation, used for the analysis of the volatile components in aged flue-cured tobacco leaves
- ↑ Extraction of essential oil from discarded tobacco leaves by solvent extraction and steam distillation, and identification of its chemical composition
- ↑ Volatile Flavor Components of Corn Tortillas and Related Products
- ↑ Volatile flavor compounds of Matsutake-Tricholomam atsutake (Ito et Imai) Sing.
- ↑ BitterDB
- ↑ Medical Subject Headings, 15 Màr 2018, C038699