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About This Item
Linear Formula:
SOCl2
CAS Number:
Molecular Weight:
118.97
Beilstein:
1209273
EC Number:
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
vapor pressure
97 mmHg ( 20 °C)
Assay
≥98%
refractive index
n20/D 1.518 (lit.)
bp
79 °C (lit.)
mp
−105 °C (lit.)
density
1.631 g/mL at 25 °C (lit.)
SMILES string
ClS(Cl)=O
InChI
1S/Cl2OS/c1-4(2)3
InChI key
FYSNRJHAOHDILO-UHFFFAOYSA-N
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General description
appearance: colorless-yellowish, clear liquid
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3
Target Organs
Respiratory system
Supplementary Hazards
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Xun Tong et al.
Soft matter, 15(31), 6411-6417 (2019-07-25)
Photoresponsive supramolecular gels have aroused continuous attention because of their extensive applications; however, most studies utilize UV light, which inevitably brings about some health and environmental issues. The halogen bond is an important driving force for constructing supramolecules due to
Feng Xu et al.
The Journal of organic chemistry, 73(1), 312-315 (2007-12-07)
A simple, one-pot preparation of cyclic amines via efficient chlorination of amino alcohols with use of SOCl(2) has been developed. This approach obviates the need for the classical N-protection/O-activation/cyclization/deprotection sequence commonly employed for this type of transformation. The reaction pathways
Hend N Hafez et al.
Bioorganic & medicinal chemistry letters, 19(15), 4143-4147 (2009-06-23)
Chlorosulfonation of 3-methyl[1,2,4]triazolo[4,3-a]pyrimidine with chlorosulfonic acid in the presence of thionyl chloride was studied. When triazolo[4,3-a]pyrimidines are used as substrates, the substitution occurs at C-6. Also the reactivity of the hydrazides (7) towards aldehydes, thioglycolic acid and amines were studies.
Gwenaël Chamoulaud et al.
Langmuir : the ACS journal of surfaces and colloids, 20(12), 4989-4995 (2005-06-30)
This paper describes a novel approach for the surface modification of a cation-exchange membrane, bearing sulfonate groups, by a cationic layer. The modification procedure involved the chlorosulfonation of the sulfonate groups of the base membrane with thionyl chloride, followed by
Alexei Chichinin et al.
Physical chemistry chemical physics : PCCP, 7(2), 301-309 (2005-01-21)
New theoretical and experimental results for the ultraviolet photodissociation dynamics of thionyl chloride (SOCl2) are presented and combined with existing data from a variety of sources in order to provide a unified view of the photodissociation dynamics of SOC12. Time-dependent
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