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MilliporeSigma

447285

Sigma-Aldrich

Thionyl chloride

ReagentPlus®, 99.5%, low iron

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About This Item

Fórmula lineal:
SOCl2
Número de CAS:
Peso molecular:
118.97
Beilstein/REAXYS Number:
1209273
EC Number:
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.21

vapor pressure

97 mmHg ( 20 °C)

Quality Level

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

SMILES string

ClS(Cl)=O

InChI

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

InChI key

FYSNRJHAOHDILO-UHFFFAOYSA-N

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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:
  • 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

Legal Information

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

For use with

Referencia del producto
Descripción
Precios

pictograms

Skull and crossbonesCorrosion

signalword

Danger

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

Storage Class

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

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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


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Los clientes también vieron

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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)
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)
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)

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