447285
氯化亚砜
ReagentPlus®, 99.5%, low iron
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线性分子式:
SOCl2
化学文摘社编号:
分子量:
118.97
UNSPSC Code:
12352300
NACRES:
NA.21
PubChem Substance ID:
EC Number:
231-748-8
Beilstein/REAXYS Number:
1209273
MDL number:
Assay:
99.5%
Form:
liquid
产品名称
氯化亚砜, ReagentPlus®, 99.5%, low iron
InChI key
FYSNRJHAOHDILO-UHFFFAOYSA-N
InChI
1S/Cl2OS/c1-4(2)3
SMILES string
ClS(Cl)=O
vapor pressure
97 mmHg ( 20 °C)
product line
ReagentPlus®
assay
99.5%
form
liquid
contains
<5 ppm iron
refractive index
n20/D 1.518 (lit.)
bp
79 °C (lit.)
mp
−105 °C (lit.)
density
1.631 g/mL at 25 °C (lit.)
cation traces
Fe: ≤5.0 ppm
Quality Level
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Application
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
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3
target_organs
Respiratory system
supp_hazards
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
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)
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)
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)
Thionyl chloride assisted functionalization of amorphous carbon nanotubes: A better field emitter and stable nanofluid with better thermal conductivity.
Sarkar SK, et al.
Materials Research Bulletin, 66, 1-8 (2015)
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