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Key Documents

447285

Sigma-Aldrich

氯化亚砜

ReagentPlus®, 99.5%, low iron

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About This Item

線性公式:
SOCl2
CAS號碼:
分子量::
118.97
Beilstein:
1209273
EC號碼:
MDL號碼:
分類程式碼代碼:
12352300
PubChem物質ID:
NACRES:
NA.21

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:
  • 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.
It may be used in the synthesis of:
  • 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

產品號碼
描述
訂價

象形圖

CorrosionSkull and crossbones

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


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Eagleson M.
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.
Palmer KJ.
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.
Zhang J, et al.
Tetrahedron Letters, 54(18), 2261-2263 (2013)
High-resolution synchrotron far infrared spectroscopy of thionyl chloride: Analysis of the ν3 and ν6 fundamental bands.
Martin-Drumel MA, et al.
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.
Li T, et al.
Synthetic Communications, 45(10), 1183-1189 (2015)

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