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Merck
CN

320544

氯化亚砜

ReagentPlus®, ≥99%

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线性分子式:
SOCl2
化学文摘社编号:
分子量:
118.97
EC Number:
231-748-8
UNSPSC Code:
12352300
PubChem Substance ID:
Beilstein/REAXYS Number:
1209273
MDL number:
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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%

form

liquid

refractive index

n20/D 1.518 (lit.)

bp

79 °C (lit.)

mp

−105 °C (lit.)

density

1.631 g/mL at 25 °C (lit.)

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Legal Information

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

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

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

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Eagleson M.
Concise Encyclopedia Chemistry, 118-118 (1994)
Jinjian Zheng et al.
Analytica chimica acta, 891, 255-260 (2015-09-22)
Thionyl chloride is often used to convert alcohols into more reactive alkyl chloride, which can be easily converted to many compounds that are not possible from alcohols directly. One important reaction of alkyl chloride is nucleophilic substitution, which is typically
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, 7-7 (1994)

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