496901
4-Methyldibenzothiophene
96%
๋ก๊ทธ์ธ์กฐ์ง ๋ฐ ๊ณ์ฝ ๊ฐ๊ฒฉ ๋ณด๊ธฐ
ํฌ๊ธฐ ์ ํ
์ ํ์ ๋ณด (DICE ๋ฐฐ์ก ์ ๋น์ฉ ๋ณ๋)
์คํ์(Hill ํ๊ธฐ๋ฒ):
C13H10S
CAS ๋ฒํธ:
Molecular Weight:
198.28
MDL number:
UNSPSC ์ฝ๋:
12352100
PubChem Substance ID:
NACRES:
NA.22
๊ธฐ์ ์๋น์ค
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๋์ ๋ฌธ์๊ธฐ์ ์๋น์ค
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๋์ ๋ฌธ์Quality Level
๋ถ์
96%
bp
298 ยฐC (lit.)
mp
64-68 ยฐC (lit.)
SMILES string
Cc1cccc2c3ccccc3sc12
InChI
1S/C13H10S/c1-9-5-4-7-11-10-6-2-3-8-12(10)14-13(9)11/h2-8H,1H3
InChI key
NICUQYHIOMMFGV-UHFFFAOYSA-N
๊ด๋ จ ์นดํ ๊ณ ๋ฆฌ
์ผ๋ฐ ์ค๋ช
4-Methyldibenzothiophene (MDBT) is a refractory sulfur compound found in fuels. Its gas-phase molar enthalpy of formation has been derived. The hydrodesulfurization (HDS) of MDBT under various conditions have been reported.
์ ํ๋ฆฌ์ผ์ด์
4-Methyldibenzothiophene (MDBT) may be used in the synthesis of the following 2-substituted products:
- 2-(3โฒ-carboxypropanoyl)-4-methyldibenzothiophene
- 2-acetyl-4-methyldibenzothiophene
- 2-nitro-4-methyldibenzothiophene
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (ยฐF)
Not applicable
Flash Point (ยฐC)
Not applicable
๊ฐ์ธ ๋ณดํธ ์ฅ๋น
Eyeshields, Gloves, type N95 (US)
๊ฐ์ฅ ์ต์ ๋ฒ์ ์ค ํ๋๋ฅผ ์ ํํ์ธ์:
์ด ์ ํ์ ์ด๋ฏธ ๊ฐ์ง๊ณ ๊ณ์ญ๋๊น?
๋ฌธ์ ๋ผ์ด๋ธ๋ฌ๋ฆฌ์์ ์ต๊ทผ์ ๊ตฌ๋งคํ ์ ํ์ ๋ํ ๋ฌธ์๋ฅผ ์ฐพ์๋ณด์ธ์.
Synthesis of supported SiW12O40-based ionic liquid catalyst induced solvent-free oxidative deep-desulfurization of fuels.
Xun S, et al.
Chemical Engineering Journal, 288, 608-617 (2016)
Hydrodesulfurization of sulfur-containing polyaromatic compounds in light oil.
Kabe T, et al.
Industrial & Engineering Chemistry Research, 31(6), 1577-1580 (1992)
Hydrodesulfurization of 4-Methyldibenzothiophene and 4,6-dimethyldibenzothiophene on a CoMo/Al2O3 catalyst: Reaction network and kinetics.
Vanrysselberghe V, et al.
Industrial & Engineering Chemistry Research, 37(4), 1235-1242 (1998)
Molecular energetics of 4-methyldibenzothiophene: An experimental study.
Freitas VLS, et al.
The Journal of Chemical Thermodynamics, 42(2), 251-255 (2010)
Substitution reactions of 4-methyldibenzothiophene.
Campaigne E, et al.
Journal of Heterocyclic Chemistry, 6(4), 553-557 (1969)
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