Neidio i'r cynnwys

cyclopentadiene

Ni chefnogir cynnwys y dudalen mewn ieithoedd eraill.

chemical compound

Adnoddau allanol

Rhif Cofrestru CAS
Reaxys registry number
471171[1]
ZVG number
DSSTOX compound identifier
UniChem compound ID
UNII
dynodwr ICSC
PubChem CID
Gmelin number
1311
OpenAlex ID
ChEMBL ID
Nikkaji ID
InChIKey
dynodwr HMDB
EC number
208-835-4[3]
ChEBI ID
30664[1][10]

mapping relation type: exact match

ChemSpider ID
J-GLOBAL ID
Cannabis Database ID
rhif RTECS
GY1000000
InChI
AICS Chemical ID (BEING DELETED)
dynodwr Freebase
DSSTox substance ID
dynodwr Microsoft Academic
Great Russian Encyclopedia Online ID (old version)
KNApSAcK ID
ECHA Substance Infocard ID
OSHA Occupational Chemical Database ID
dynodwr Encyclopædia Universalis
NMRShiftDB structure ID
CAMEO Chemicals ID
Great Russian Encyclopedia portal ID
Encyclopedia of China (Third Edition) ID
dynodwr HSDB

enghraifft o'r canlynol

math o endid cemegol

isddosbarth o'r canlynol

monoprotic acid
diene
carbon acid
cyclic compound

adeiledd gemegol

image of molecular model or crystal lattice model

yn portreadu: space-filling model

yn portreadu: ball-and-stick model

màs

66.047 uned Dalton[5]

associated hazard

cyclopentadiene exposure

effaith

cyclopentadiene exposure[16]

conjugate base

cyclopentadienide

fformwla gemegol

C₅H₆[5]

SMILES

C1C=CC=C1[5]

ionization energy

8.56±0.01 electronvolt[16][17]

trefnolyn: 1

electric dipole moment

0.419 debye[17]

dwysedd

0.8±0.01 gram per cubic centimetre[16]

tymheredd: 20±1 gradd Celsius

ymdoddbwynt

−121±1 gradd Fahrenheit[16]
−85 gradd Celsius[17]

boiling point

107±1 gradd Fahrenheit[16]

under pressure: 760±1 torr

41 gradd Celsius[17]

under pressure: 101.325 kilopascal

vapor pressure

400±1 millimetre of mercury[16]

tymheredd: 68±1 gradd Fahrenheit

flash point

77±1 gradd Fahrenheit[16]

dull penderfynu: Cleveland open-cup method

NIOSH Pocket Guide ID

0170

time-weighted average exposure limit

200±1 milligram per cubic metre[16]

hyd (amser): 10±1 awr

yn perthyn i'r awdurdod canlynol: Unol Daleithiau America

immediately dangerous to life or health

2,025±1 milligram per cubic metre[16]

found in taxon

Cymbopogon citratus[18]
Oryza sativa[19]

nodwedd o'r endid

Class IC flammable liquid[16]

yn cynnwys

yn wahanol i

cyclopentadienide

categori Comin

Cyclopentadiene

Cyfeiriadau

  1. 1.0 1.1 1.2 ChEBI, 6 Hydref 2016, Saesneg, cyclopentadiene, 30664
  2. UniChem
  3. 3.0 3.1 Global Substance Registration System, 6 Hydref 2016, Saesneg, CYCLOPENTADIENE, 5DFH9434HF
  4. 4.0 4.1 4.2 4.3 4.4 4.5 ZSWFCLXCOIISFI-UHFFFAOYSA-N, InChIKey
  5. 5.0 5.1 5.2 5.3 5.4 5.5 PubChem, 6 Hydref 2016, Saesneg, 7612, Cyclopentadiene
  6. OpenAlex, 26 Ionawr 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  7. ChEMBL, 6 Hydref 2016, Saesneg, CHEMBL3188826, CHEMBL3188826
  8. ChEBI release 2020-09-01
  9. 9.0 9.1 inferred from InChIKey
  10. International Chemical Identifier, InChI=1S/C5H6/c1-2-4-5-3-1/h1-4H,5H2
  11. ChemSpider, 6 Hydref 2016, Saesneg, 7330, Cyclopentadiene
  12. Cannabis Database
  13. Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
  14. ECHA Substance Infocard database, 27 Rhagfyr 2018, 100.008.033, Cyclopentadiene, CAS no.: 542-92-7
  15. Hazardous Substances Data Bank, 10 Mai 2021, 28 Hydref 2019, 1,3-CYCLOPENTADIENE, 2514
  16. 16.00 16.01 16.02 16.03 16.04 16.05 16.06 16.07 16.08 16.09 http://www.cdc.gov/niosh/npg/npgd0170.html
  17. 17.0 17.1 17.2 17.3 Basic laboratory and industrial chemicals: A CRC quick reference handbook
  18. GC-MS evaluation of Cymbopogon citratus (DC) Stapf oil obtained using modified hydrodistillation and microwave extraction methods
  19. Bio-fuel oil characteristic of rice bran wax pyrolysis