| Identification | Back Directory | [Name]
1,4,6-ANDROSTATRIEN-3,17-DIONE | [CAS]
144413-58-1 | [Synonyms]
ADT
ATD
ADT sublimed, 97%
ANDROSTATRIENEDIONE
ADT AldrichCPR, sublimed
1,4,6-ANDROSTATRIEN-3,17-DIONE
Anthra[2,3-b:6,7-b']dithiophene
Anthra[2,3-b :6,7-b' ]dithiophene
androsta-1,4,6-triene-3,17-dione(androstatrienedione) | [Molecular Formula]
C18H10S2 | [MDL Number]
MFCD00271207 | [MOL File]
144413-58-1.mol | [Molecular Weight]
290.4 |
| Chemical Properties | Back Directory | [Boiling point ]
534.8±23.0 °C(Predicted) | [density ]
1.417±0.06 g/cm3(Predicted) | [form ]
sublimed | [semiconductor properties]
P-type (mobility=0.3cm2/V·s) | [λmax]
320 nm in methylene chloride | [InChI]
1S/C18H10S2/c1-3-19-17-9-15-8-14-6-12-2-4-20-18(12)10-16(14)7-13(15)5-11(1)17/h1-10H | [InChIKey]
DAMUWSYTQPWFIY-UHFFFAOYSA-N | [SMILES]
c1cc2cc3cc4cc5sccc5cc4cc3cc2s1 |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
22 | [WGK Germany ]
3 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Acute Tox. 4 Oral |
| Hazard Information | Back Directory | [Uses]
ADT can be used as a conducting polymer in the fabrication of organic field effect transistors (OFETs) and organic photovoltaics (OPVs). | [General Description]
ADT is an anthradithiophene based small molecule semiconductor that contributes to a new class of heteroacenes, which has a 22-electron π-conjugated system. It can be majorly used in a variety of organic electronic applications. |
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