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????? ??? ???
?? ??:
95-15-8
???:
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???(??):
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Thianaphthene
???(??):
BENZO[B]THIOPHENE;BENZOTHIOPHENE;BBT;BZT;THIONAPHTHENE;1-BENZOTHIOPHENE;Thianapthene;Thionaphthalene;Thiaphthene;ianaphthene
CBNumber:
CB0683988
???:
C8H6S
??? ??:
134.2
MOL ??:
95-15-8.mol
MSDS ??:
SDS

????? ??

???
30-33 °C
?? ?
221-222 °C(lit.)
??
1.149 g/mL at 25 °C(lit.)
???
1.33 hPa ( 20 °C)
???
1.6332 (estimate)
???
>230 °F
?? ??
Store below +30°C.
???
0.13g/L
??? ??
??? ??
?? ?? (pKa)
32.4
Specific Gravity
1.149
??
???? ??? ?? ?????
???
???
Merck
14,9303
BRN
80580
Henry's Law Constant
4.1×10-2 mol/(m3Pa) at 25℃, Mackay et al. (1995)
InChI
1S/C8H6S/c1-2-4-8-7(3-1)5-6-9-8/h1-6H
InChIKey
FCEHBMOGCRZNNI-UHFFFAOYSA-N
SMILES
c1ccc2sccc2c1
LogP
3.120
CAS ??????
95-15-8(CAS DataBase Reference)
NIST
Benzo[b]thiophene(95-15-8)
EPA
Benzo[b]thiophene (95-15-8)
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? Xn,Xi,N
?? ???? ?? 22-36/37/38-20/21/22-51/53
????? 22-24/25-36-26-61
????(UN No.) UN3077
WGK ?? 3
?? ?? ?? 510°C
?? ?? ?? Irritant
TSCA TSCA listed
?? ?? 9
???? III
HS ?? 29349990
???? ??? 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
Aquatic Chronic 3
???? ?? 2017-3-7221
????(GHS): Exclamation Mark (GHS07)
?? ?: Warning
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H302 ??? ??? ?? ?? ?? - ?? ?? 4 ?? P264, P270, P301+P312, P330, P501
H412 ??? ??? ?? ????? ??? ?? ????? ?? - ?? ?? 3 P273, P501
??????:
P264 ?? ??? ?? ??? ????.
P264 ?? ??? ?? ??? ????.
P270 ? ??? ??? ??? ???, ???? ???? ???.
P273 ???? ???? ???.
P301+P312 ??? ???? ??? ????(??)? ??? ????.
P501 ...? ??? / ??? ?? ???.
NFPA 704
1
2 0

????? MSDS


Thianaphthene

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WHITE TO RED CRYSTALLINE LOW MELTING SOLID

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Thianaphthene may be used in the preparation of 2-thianapthenylphenyllithium, via metalation by n-butyllithium.

?? ??

Thianaphthene may be used in the preparation of 2-thianapthenylphenyllithium, via metalation by n-butyllithium.
Reaction of ethyl diazoacetate with thianaphthene has been reported.

?? ??

Reaction of ethyl diazoacetate with thianaphthene has been reported.

Purification Methods

1-Benzothiophene has the odour of naphthalene. If the IR spectrum is not very good, then suspend it in a faintly alkaline aqueous solution and steam distil it. Extract the distillate with Et2O, dry the extract (CaCl2), filter, evaporate the solvent and fractionate the residue. The distillate sets solid. The sulfoxide has m 142o, the picrate has m 148-149o (yellow crystals from EtOH) and the styphnate has m 136-137o. [Hansch & Lindwall J Org Chem 10, 381 1945, Meyer & Meyer Chem Ber 52B 1249 1919, Weisgerber & Kruber 53 1551 1920, Iddon & Scrowston Adv Heterocycl Chem 11 177 1970, Beilstein 17/2 V 6.]

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