| Identification | Back Directory | [Name]
BENZO(B)NAPHTHO(2,1-D)THIOPHENE | [CAS]
239-35-0 | [Synonyms]
11-thiabenzo(a)fluorene
1,2-Benzo-9-thiafluorene
Benzo[a]dibenzothiophene
3,4-Benzodibenzothiophene
Naphtho[1,2-b]thianaphthene
1,2-BENZODIPHENYLENE SULFIDE
naphtho[1,2-b][1]benzothiole
naphtho[1,2-b]benzothiophene
naphtho(1,2:2,3)thionaphthen
BENZONAPHTHO(2,1-D)THIOPHENE
BENZO(B)NAPH(2,1-D)THIOPHENE
BENZO[B]NAPHTHO[2,1-D]THIOPH
Benzo[b]naphtho[2,1]thiophene
1,2-BENZODIPHENYLENE SULPHIDE
benzo[b]naphto[2,1-d]thiophene
Naphtho[1,2-b][1]benzothiophene
BENZO(B)NAPHTHO(2,1-D)THIOPHENE
1,2-Benzodiphenylene sulfide 99%
1,2-BENZODIPHENYLENE SULPHIDE 99%
3,4-[1,3]Butadienodibenzothiophene
3,4-(1,3-Butadiene-1,4-diyl)dibenzothiophene
1,2-Benzodiphenylene sulfide,Benzo[b]naphtho[2,1-d]thiophene | [EINECS(EC#)]
205-948-0 | [Molecular Formula]
C16H10S | [MDL Number]
MFCD00010043 | [MOL File]
239-35-0.mol | [Molecular Weight]
234.32 |
| Chemical Properties | Back Directory | [Melting point ]
188-190 °C(lit.) | [Boiling point ]
434.3±14.0 °C(Predicted) | [density ]
1.292±0.06 g/cm3(Predicted) | [solubility ]
chloroform: soluble2.5%, clear to very slightly hazy, colorless to faint yellow or tan | [form ]
solid | [InChI]
1S/C16H10S/c1-2-6-12-11(5-1)9-10-14-13-7-3-4-8-15(13)17-16(12)14/h1-10H | [InChIKey]
YEUHHUCOSQOCIX-UHFFFAOYSA-N | [SMILES]
c1ccc2c(c1)ccc3c4ccccc4sc23 | [IARC]
3 (Vol. 103) 2013 | [EPA Substance Registry System]
Benzo[b]naphtho[2,1-d]thiophene (239-35-0) |
| Hazard Information | Back Directory | [Uses]
1,2-Benzodiphenylene sulfide has been used in direct screening of sediment samples for polycyclic aromatic hydrocarbons by flow manifold coupled on-line to a fluorimetric detector. | [Definition]
ChEBI: Benzo[b]naphtho[2,1-d]thiophene is an organosulfur heterocyclic compound and an organic heterotricyclic compound. | [General Description]
1,2-benzodiphenylene sulfide is a rare constituent of coal tar. Photodeoxygenation of 1,2-benzodiphenylene sulfoxide, generates an intermediate capable of oxidizing the solvent benzene to phenol. Liquid-phase photolysis of 1,2-benzodiphenylene sulfide to generate atomic oxygen [O(3P)] or an equivalent active oxygen species has been reported. |
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