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化驗
97%
折射率
n20/D 1.628 (lit.)
bp
124-125 °C/10 mmHg (lit.)
密度
1.51 g/mL at 25 °C (lit.)
SMILES 字串
CSc1cccc(Br)c1
InChI
1S/C7H7BrS/c1-9-7-4-2-3-6(8)5-7/h2-5H,1H3
InChI 密鑰
NKYFJZAKUPSUSH-UHFFFAOYSA-N
一般說明
3-Bromothioanisole is a 3-halothioanisole derivative that is mainly used in the preparation of photoacids. It can be prepared from 3-bromobenzenethiol.
應用
3-Bromothioanisole may be used in the preparation of:
- 3-methylthiotriphenylamine
- 4-ethoxy-3′-methylthiostilbene
- 3-bromophenyl phenyl sulfide
- 9-substituted, 3,6-dithiomethylfluorenes
- 4-methoxy-3′-(methylthio)-1,1′-biphenyl
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
230.0 °F - closed cup
閃點（°C）
110 °C - closed cup
個人防護裝備
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Enhancement of acid photogeneration through a para-to-meta substitution strategy in a sulfonium-based alkoxystilbene designed for two-photon polymerization.
Xia R, et al.
Chemistry of Materials, 24(2), 237-244 (2012)
Evaluating atomic components in fluorene wires.
Klausen RS, et al.
Chemical Science, 5(4), 1561-1564 (2014)
Efficient photoacids based upon triarylamine dialkylsulfonium salts.
Zhou W, et al.
Journal of the American Chemical Society, 124(9), 1897-1901 (2002)
A Preparatively Convenient Ligand-Free Catalytic PEG 2000 Suzuki- Miyaura Coupling.
Razler TM, et al.
The Journal of Organic Chemistry, 74(3), 1381-1384 (2008)
Transition-Metal-Free Acid-Mediated Synthesis of Aryl Sulfides from Thiols and Thioethers.
Wagner AM and Sanford MS.
The Journal of Organic Chemistry, 79(5), 2263-2267 (2014)
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