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Sigma-Aldrich

Thionyl chloride solution

2.0 M in methylene chloride

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Linear Formula:
SOCl2
CAS Number:
Molecular Weight:
118.97
MDL number:
PubChem Substance ID:
NACRES:
NA.21

vapor pressure

97 mmHg ( 20 °C)

Quality Level

form

liquid

concentration

2.0 M in methylene chloride

density

1.373 g/mL at 25 °C

SMILES string

ClS(Cl)=O

InChI

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

InChI key

FYSNRJHAOHDILO-UHFFFAOYSA-N

Related Categories

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Skin Corr. 1A

supp_hazards

Storage Class

6.1B - Non-combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 2

flash_point_c

Not applicable


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Eagleson M.
Concise Encyclopedia Chemistry, 1056-1056 (1994)
Meng Zhou et al.
Molecules (Basel, Switzerland), 20(6), 10122-10130 (2015-06-04)
Pincer (Phebox)Ir(mesityl)(OAc) (2) (Phebox = 3,5-dimethylphenyl-2,6-bis(oxazolinyl)) complex, formed by benzylic C-H activation of mesitylene (1,3,5-trimethylbenzene) using (Phebox)Ir(OAc)2OH2 (1), was treated with thionyl chloride to rapidly form 1-(chloromethyl)-3,5-dimethylbenzene in 50% yield at 23 °C. A green species was obtained at the
Eagleson M.
Concise Encyclopedia Chemistry, 118-118 (1994)
Eagleson M.
Concise Encyclopedia Chemistry, 1049-1049 (1994)
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

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