1,3-benzenedithiol

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Names

[ CAS No. ]:
626-04-0

[ Name ]:
1,3-benzenedithiol

[Synonym ]:
benzene-1,3-dithiol
MFCD00004842
EINECS 210-925-3

Chemical & Physical Properties

[ Boiling Point ]:
128-129 °C16 mm Hg(lit.)

[ Melting Point ]:
24-25 °C(lit.)

[ Molecular Formula ]:
C6H6S2

[ Molecular Weight ]:
142.24200

[ Flash Point ]:
>230 °F

[ Exact Mass ]:
141.99100

[ PSA ]:
77.60000

[ LogP ]:
2.26400

[ Index of Refraction ]:
1.665

Safety Information

[ Symbol ]:

GHS05, GHS07

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H315-H318-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R20/21/22;R36/38

[ Safety Phrases ]:
S26-S39

[ RIDADR ]:
PG 3

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ HS Code ]:
2930909090

Synthetic Route

Click to get detail synthetic route

Customs

[ HS Code ]: 2930909090

[ Summary ]:
2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Performance enhancement of hybrid solar cells through chemical vapor annealing.

Nano Lett. 10(5) , 1628-31, (2010)

Improvement in power conversion efficiency has been observed in cadmium selenide nanorods/poly(3-hexylthiophene) hybrid solar cells through benzene-1,3-dithiol chemical vapor annealing. Phosphor NMR s...

Photovoltaic Performance of PbS Quantum Dots Treated with Metal Salts.

ACS Nano 10 , 3382-8, (2016)

Recent advances in quantum dot surface passivation have led to a rapid development of high-efficiency solar cells. Another critical element for achieving efficient power conversion is the charge neutr...


More Articles

Related Compounds

  • 4-chloro-1,3-benzenedithiol
  • 1,3-Benzenedithiol,4,6-dichloro
  • 1-[3-(N-benzylanilino)-2-pyrrolidin-1-ylpropoxy]-2-methylpropan-2-ol
  • 1-(3-chloropropyl)-4-phenoxybenzene
  • 1,3,5-Triazine,2-(2-chloroethyl)-4,6-bis(trichloromethyl)-
  • (-)-1-(3-Ethylphenyl)-2-pyrrolidinemethanamine fumarate
  • 6-(4-{3-Methyl-[1,2,4]triazolo[4,3-b]pyridazin-6-yl}-1,4-diazepan-1-yl)pyridine-3-carbonitrile
  • 1-{3-Methyl-[1,2,4]triazolo[4,3-b]pyridazin-6-yl}-4-(4-methylthiophene-2-carbonyl)-1,4-diazepane
  • N-(3-Chlorophenyl)-3-(triazol-2-yl)azetidine-1-carboxamide
  • 4-({5H,6H,7H-cyclopenta[c]pyridazin-3-yloxy}methyl)-1-(1H-imidazole-4-sulfonyl)piperidine
  • 4-Cyclobutylidene-1-(3,4-difluorobenzenesulfonyl)piperidine
  • 3-chloro-N-[2-hydroxy-4-(methylsulfanyl)butyl]-4-methylbenzene-1-sulfonamide
  • 1-(3,4-Dimethylphenyl)-4-[2-(2-methylpyrazol-3-yl)piperidine-1-carbonyl]pyrrolidin-2-one
  • N-phenyl-3-[(1H-1,2,3-triazol-1-yl)methyl]azetidine-1-carboxamide
  • N-(5-chloro-2-methoxyphenyl)-3-(2H-1,2,3-triazol-2-yl)azetidine-1-carboxamide
  • N-Phenyl-3-(1,2,5-thiadiazol-3-yloxy)pyrrolidine-1-carboxamide
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