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Merck
CN

447285

Sigma-Aldrich

氯化亚砜

ReagentPlus®, 99.5%, low iron

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关于此项目

线性分子式:
SOCl2
CAS Number:
分子量:
118.97
Beilstein:
1209273
EC 号:
MDL编号:
UNSPSC代码:
12352300
PubChem化学物质编号:
NACRES:
NA.21
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蒸汽压

97 mmHg ( 20 °C)

质量水平

产品线

ReagentPlus®

方案

99.5%

表单

liquid

包含

<5 ppm iron

折射率

n20/D 1.518 (lit.)

沸点

79 °C (lit.)

mp

−105 °C (lit.)

密度

1.631 g/mL at 25 °C (lit.)

痕量阳离子

Fe: ≤5.0 ppm

SMILES字符串

ClS(Cl)=O

InChI

1S/Cl2OS/c1-4(2)3

InChI key

FYSNRJHAOHDILO-UHFFFAOYSA-N

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应用

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

法律信息

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

象形图

Skull and crossbonesCorrosion

警示用语:

Danger

危险分类

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3

靶器官

Respiratory system

补充剂危害

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
Eagleson M.
Concise Encyclopedia Chemistry, 7-7 (1994)
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)
Synthesis and characterization of some novel stilbene derivatives derived from substituted (phenyl acetic acid, benzaldehyde, amines) triethyl amine and thionyl chloride.
More PS and Singh SG.
International Letters of Chemistry, Physics and Astronomy, 4, 71-71 (2015)

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