推薦產品
蒸汽壓力
97 mmHg ( 20 °C)
品質等級
產品線
ReagentPlus®
化驗
99.5%
形狀
liquid
包含
<5 ppm iron
折射率
n20/D 1.518 (lit.)
bp
79 °C (lit.)
mp
−105 °C (lit.)
密度
1.631 g/mL at 25 °C (lit.)
正離子痕跡
Fe: ≤5.0 ppm
SMILES 字串
ClS(Cl)=O
InChI
1S/Cl2OS/c1-4(2)3
InChI 密鑰
FYSNRJHAOHDILO-UHFFFAOYSA-N
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應用
Thionyl chloride was used to produce graphene-based hybrid transparent conductive electrodes (TCEs).
It may be used in the following processes:
It may be used in the following processes:
- Synthesis of indenones from 3-hydroxyindanones via dehydroxylation.
- Modification of amorphous carbon nanotubes (a-CNTs) in stearic acid-dichloro methane solution.
- To functionalize silica gel for thioacetalization of aldehydes.
- substituted stilbene derivatives
- tert-butyl ((S)-1-((R)-oxiran-2-yl)-2-phenylethyl)carbamate
- optically active chloroalkanes
法律資訊
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
附屬品
訊號詞
Danger
危險分類
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3
標靶器官
Respiratory system
安全危害
儲存類別代碼
6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
水污染物質分類(WGK)
WGK 1
閃點(°F)
Not applicable
閃點(°C)
Not applicable
個人防護裝備
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
客戶也查看了
Concise Encyclopedia Chemistry, 7-7 (1994)
The electron diffraction investigation of sulfur monochloride, sulfur dichloride, sulfur trioxide, thionyl chloride, sulfuryl chloride, vanadium oxytrichloride, and chromyl chloride.
Journal of the American Chemical Society, 60(10), 2360-2369 (1938)
CaF2 catalyzed SN2 type chlorodehydroxylation of chiral secondary alcohols with thionyl chloride: a practical and convenient approach for the preparation of optically active chloroalkanes.
Tetrahedron Letters, 54(18), 2261-2263 (2013)
High-resolution synchrotron far infrared spectroscopy of thionyl chloride: Analysis of the ν3 and ν6 fundamental bands.
Journal of Molecular Spectroscopy (2015)
Thionyl Chloride-Mediated Synthesis of tert-Butyl ((S)-1-((R)-Oxiran-2-yl)-2-phenylethyl) carbamate with Boc-Involved Neighboring Group Participation.
Synthetic Communications, 45(10), 1183-1189 (2015)
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