furfural

kjemisk forbindelse

Eksterne ressurser

Art & Architecture Thesaurus-ID
ZVG-nummer
HCIS ID
DSSTOX compound identifier
Encyclopædia Britannica Online-ID
science/furfural

namain: furfural

NSC-numero
ChEMBL-ID
Gran Enciclopèdia Catalana -tunniste
HMDB-ID
Römpp online -tunniste
MeSH-kode
AICS Chemical ID (BEING DELETED)
RTECS-nummer
LT7000000
ECHA InfoCard -tunniste
UM-BBD compound ID
PDB ID
FEMA number
CAMEO Chemicals ID
NALT-gilkor
Encyclopedia of China (Third Edition) ID
Probes And Drugs ID
De Agostini ID
furfurale

namain: furfurale

Freebase-gilkor
CA PROP 65 ID
Microsoft Academic-ID
UniChem compound ID
UNII
Quora-fáddágilkor
YSO-gilkor
WordNet 3.1 Synset ID
14900624-n
PDB ligand ID
SPLASH
PesticideInfo chemical ID
DSSTox substance ID
MassBank accession ID
KEGG-ID
OpenAlex-ID
InChI
EU-nummer
202-627-7[12]
LCAuth-gilkor
InChIKey
Cannabis Database ID
ChEBI-ID
34768[16][21]

SKOS-relasjonstype: eksakt samsvar

CosIng-tunnistenumero
Gran Enciclopèdia Catalana-ID
CAS-nummer
Reaxys registry number
105755[16]
SNL-gilkor
PubChem-id (CID)
ICSC ID
MeSH-ID
D005662

namain: Furaldehyde

NDL-nummer
KNApSAcK-tunniste
UMLS CUI
JECFA number
450[25]
FL number
13.018[26]
OSHA Occupational Chemical Database ID
ChemSpider-ID
JECFA database ID
NMRShiftDB structure ID
NKC-gilkor
ph314893

namain: furfural

GND-gilkor
National Library of Israel J9U ID
HSDB-tunniste

lea

type kjemisk entitet

gullá čuovvovaš kategoriijai

heterosyklisk forbindelse
aldehyd

del av

response to furfural[30]

subjekt har rollen: reaktant

furaldehyde metabolic process[31]

subjekt har rollen: participant

kjemisk struktur

masse

96,021 atommasseenhet[18]

čuovvumušat

furfural exposure[32]

kjemisk formel

C₅H₄O₂[18]

SMILES

C1=COC(=C1)C=O[18]

ioniseringsenergi

9,21±0,01 elektronvolt[32][33]

sadji ráiddus: 1

tetthet

1,16±0,01 grammaa per kuutiosenttimetri[32]

temperatuvra: 20±1 grader celsius

smeltepunkt

−34±1 grader fahrenheit[32]
−38 grader celsius[34]
−36,5 grader celsius[33]

kokepunkt

323±1 grader fahrenheit[32]

trykk: 760±1 torr

161,75 grader celsius[33]

trykk: 101,325 kilopascal

damptrykk

2±1 millimeter kvikksølv[32]

temperatuvra: 68±1 grader fahrenheit

løselighet

8±1 gram per 100 gram of solvent[32]

temperatuvra: 68±1 grader fahrenheit

løsemiddel: čáhci

flammepunkt

140±1 grader fahrenheit[32]

bestemmelsesmetode: Pensky–Martens closed-cup test

nedre eksplosjonsgrense

2,1±0,1 volumprosent[32]

øvre eksplosjonsgrense

19,3±0,1 volumprosent[32]

NIOSH Pocket Guide ID

0297

time-weighted average exposure limit

20±1 milligrammaa kuutiometrissä[32]

administrasjonsvei: hudkontakt

doaibmaváldi, masa gullá: Amerihká ovttastuvvan stáhtat

bistu: 8±1 diibmu

immediately dangerous to life or health

393±1 milligrammaa kuutiometrissä[32]

finnes i takson

mandel[35]
vandreblomst[36]
Coffea arabica[37]
Paeonia lactiflora[38]
Edelråte[39]
Sapodilletre[40]
Swertia japonica[41]
ingefær[42]
jordskokk[43]
Pueraria montana var. lobata[44]
lakrisplante[45][46]
Sitronmelisse[47]
Ruutubukko[48]
Asarum canadense[49]
havre[50]
Malabarinpinaatti[51]
Campsis grandiflora[52]
Castanopsis cuspidata[53]
Rohtosammakonputki[54]
endivie[55]
Cinnamomum zeylanicum[56]
Daphne genkwa[57]
mangostantre[58]
Geum heterocarpum[64]
Hagebønne[65]
Polygala senega[66]
Saussurea involucrata[67]
Kryddernellik[68]
Tamarind[69][70]
Kakaotre[71]
Vitis rotundifolia[72]
Kapers[73]
Streptomyces cavourensis[74]
Angelica gigas[75]
Manankukka[76]
blodkløver[77]
løkurt[78]
Streptomyces bacillaris[74]
seller[79]
papaya[80]
Garcinia dulcis[81]
gran[82]
Viherkameleonttilehti[83]
Tobakksplante[84][85]
asparges[86]
Ligusticum chuanxiong[87]
Palsamiköynnös[88]
Viburnum orientale[89]
Magnolia obovata[90]
Vetiveriaheinä[91]
Conioselinum anthriscoides[87]
Ligusticum striatum[87]
Ceyloninkaneli[56]
morell[35]
Scleromitrion diffusum[92]
febertre[93]
Eucalyptus polyanthemos[93]
Eucalyptus perriniana[93]
Ekte vinranke[94]

beskrevet i kilde

Armenske sovjetiske encyklopedi
Entsiklopeditsjeskij slovar Granat

tema for: Q87337566

har egenskap

Class IIIA combustible liquid[32]

subjekt har rollen

metabolitt

finnes i takson: Homo sapiens

dasa gullet

oksygena
čitna

Commons-kategoriija

Furfural

fáttá váldokategoriija

Luokka:Furfuraalit

Gáldu

  1. ChEMBL, 19 golggotmánnu 2016, eaŋgalsgiella, FURFURAL, CHEMBL189362
  2. a á b inferred from InChIKey
  3. a á b c HYBBIBNJHNGZAN-UHFFFAOYSA-N, InChIKey
  4. ECHA Substance Infocard database, 27 juovlamánnu 2018, 100.002.389, 2-furaldehyde, CAS no.: 98-01-1
  5. Protein Data Bank, 19 golggotmánnu 2016, eaŋgalsgiella, 1QXD, 1QXD
  6. Protein Data Bank, 19 golggotmánnu 2016, eaŋgalsgiella, 3S2F, 3S2F
  7. Protein Data Bank, 19 golggotmánnu 2016, eaŋgalsgiella, 3S2G, 3S2G
  8. Protein Data Bank, 19 golggotmánnu 2016, eaŋgalsgiella, 3S2I, 3S2I
  9. Freebase-data fra Google, 28 golggotmánnu 2013
  10. California Proposition 65 list of chemicals, 6 ođđajagimánnu 2020, https://oehha.ca.gov/chemicals/furfural
  11. UniChem
  12. a á Global Substance Registration System, 19 golggotmánnu 2016, eaŋgalsgiella, furfural, DJ1HGI319P
  13. Quora
  14. YSOn ja Wikidatan linkitys
  15. Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
  16. a á b c č ChEBI, 19 golggotmánnu 2016, eaŋgalsgiella, furfural, 34768
  17. OpenAlex, 26 ođđajagimánnu 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  18. a á b c č d PubChem, 19 golggotmánnu 2016, eaŋgalsgiella, 7362, FURFURAL
  19. ChEBI release 2020-09-01
  20. Cannabis Database
  21. International Chemical Identifier, InChI=1S/C5H4O2/c6-4-5-2-1-3-7-5/h1-4H
  22. CosIng database, 28 juovlamánnu 2019, 33965, FURFURAL, CAS no.: 98-01-1
  23. CAS Common Chemistry, 9 cuoŋománnu 2021, HYBBIBNJHNGZAN-UHFFFAOYSA-N, https://commonchemistry.cas.org/detail?cas_rn=98-01-1
  24. UMLS 2023, 24 miessemánnu 2023, inferred by common MeSH mappings on source and on Wikidata
  25. Evaluations of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 30 skábmamánnu 2021
  26. EFSA database, 23 ođđajagimánnu 2021, CAS no.: 98-01-1, 13.018
  27. ChemSpider, 19 golggotmánnu 2016, eaŋgalsgiella, 13863629, Furfural
  28. National Library of Israel Names and Subjects Authority File
  29. Hazardous Substances Data Bank, 10 miessemánnu 2021, 28 golggotmánnu 2019, FURFURAL, 542
  30. Gene Ontology release 2019-11-16
  31. Gene Ontology release 2020-05-02
  32. a á b c č d đ e f g h i j http://www.cdc.gov/niosh/npg/npgd0297.html
  33. a á b Basic laboratory and industrial chemicals: A CRC quick reference handbook
  34. Jean-Claude Bradley Open Melting Point Dataset
  35. a á Components of almond hulls: possible navel orangeworm attractants and growth inhibitors
  36. PHYTOCHEMICAL STUDY OF LANTANA CAMARA I
  37. New volatile components of roasted coffee
  38. "Essential oil constituents of \"PAEONIAE RADIX\" Peaonia lactiflora Pall. (P. albilora Pall.)."
  39. Odorous metabolites of fungi, Chaetomium globosum Kinze ex Fr. and Botrytis cinerea Pers. ex Fr., and a blue-green alga, Phormidium tenue (Meneghini) Gomont.
  40. Volatile flavor components of sapodilla fruit (Achras sapota L)
  41. Semburins and Swertiols, Novel 2,8-Dioxabicyclo[3.3.1]nonanes and Their Precursory Alcohols, fromSwertia japonicaMakino
  42. Investigation of the essential oil of Vietnamese ginger
  43. Aroma volatiles of Cynara scolymus and Helianthus tuberosus
  44. Volatile flavor components of Puerariae radix (Pueraria lobata Ohwi).
  45. Components of essential oil from the root of Glycyrrhiza glabra.
  46. Volatile flavor components of licorice
  47. The Constituents ofMelissa officinalisL. Cultures
  48. Analysis of Buchu leaf oil
  49. Composition of the essential oil from Asarum canadense
  50. Volatile food attractants forOryzaephilus surinamensis (L.) from oats
  51. Volatile flavor components of malabar-nightshade (Basella rubra L.)
  52. The essential oil from the flowers ofCampsis grandiflora (Thumb.) K. Schum. from China
  53. Volatile constituents of Castanopsis flower
  54. Essential Oil ofCentella asiatica(L.) Urb.
  55. Neutral volatiles from blended endive (Cichorium endivia, L.)
  56. a á Volatile constituents of cinnamon (Cinnamomum zeylanicum) oils
  57. The Chemical Composition of the Essential Oil ofDaphne genkwaSieb. et Zucc.
  58. Volatile flavour components of mangosteen, Garcinia mangostana
  59. Volatile aroma constituents of mango (cv Kensington)
  60. Volatile components from mango (Mangifera indica L.) cultivars
  61. Aroma Volatile Constituents of Brazilian Varieties of Mango Fruit
  62. Glycosidically-bound aroma volatile compounds in the skin and pulp of ‘Kensington Pride’ mango fruit at different stages of maturity
  63. Characteristic Aroma Components of the Volatile Oil of Yellow Keaw Mango Fruits Determined by Limited Odor Unit Method.
  64. Composition of the Root Oil ofOrthurus heterocarpus(Boiss.) Juz.
  65. Characterization of some volatile constituents of dry red beans
  66. Volatile compounds ofPolygala senega L. var.latifolia Torrey et Gray roots
  67. Components of the Essential Oil of Saussurea involucrata (Kar. et Kir.) ex Maxim
  68. Volatile components of clove essential oil (Eugenia caryophyllus SPRENG): Neutral fraction.
  69. Volatile Flavor Components of Tamarind (Tamarindus indicaL.)
  70. Supercritical Fluid Extraction of the Volatile Constituents from Tamarind (Tamarindus indicaL.)
  71. Steam volatile aroma constituents of roasted cocoa beans
  72. Identification of the Volatile Constituents from Scuppernong Berries (Vitis rotundifolia)
  73. Nematicidal activity of 2-thiophenecarboxaldehyde and methylisothiocyanate from caper (Capparis spinosa) against Meloidogyne incognita
  74. a á Biocontrol of anthracnose in pepper using chitinase, beta-1,3 glucanase, and 2-furancarboxaldehyde produced by Streptomyces cavourensis SY224
  75. Analysis of the influence of sulfur-fumigation on the volatile components of Angelicae sinensis Radix by comprehensive two-dimensional gas chromatography/time-of-flight mass spectrometry
  76. Volatile constituents of Dactylanthus taylorii flower nectar in relation to flower pollination and browsing by animals
  77. LXXIX.—The constituents of the flowers of Trifolium incarnatum
  78. Free and Bound Volatiles of Garlic Mustard (Alliaria petiolata)
  79. Aromatic Volatile Composition of Celery and Celeriac Cultivars
  80. Volatile components of papaya (Carica papaya L., Maradol variety) fruit
  81. Volatile constituents of fruits of Garcinia dulcis Kurz. from Cuba
  82. Analysis of chemical changes in Picea abies wood decayed by different Streptomyces strains showing evidence for biopulping procedures
  83. Gas chromatography–mass spectrometry analysis of volatile compounds from Houttuynia cordata Thunb after extraction by solid-phase microextraction, flash evaporation and steam distillation
  84. 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
  85. Extraction of essential oil from discarded tobacco leaves by solvent extraction and steam distillation, and identification of its chemical composition
  86. EVALUATION OF ASPARAGUS OFFICINALIS L. FLAVOUR QUALITY FOR BREEDING PURPOSES
  87. a á b Analysis of the volatile compounds in Ligusticum chuanxiong Hort. using HS-SPME-GC-MS.
  88. Analysis of volatile fractions of Schisandra chinensis (Turcz.) Baill. using GC-MS and chemometric resolution
  89. Composition of the Essential Oil from Viburnum orientale Pallas Leaves
  90. Composition of the Bark Oil of Magnolia obovata Thunb.
  91. Headspace Constituents of Vetiver Oil
  92. Composition of the Essential Oil of Hedyotis diffusa Willd.
  93. a á b Antioxidant activities of volatile components isolated from Eucalyptus species
  94. Separation and Identification of Furanic Compounds in Fruit Juices and Drinks by High-Performance Liquid Chromatography Photodiode Array Detection