293121
亚硫酰氯 溶液
2.0 M in methylene chloride
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关于此项目
线性分子式:
SOCl2
化学文摘社编号:
分子量:
118.97
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352300
MDL number:
Form:
liquid
InChI
1S/Cl2OS/c1-4(2)3
SMILES string
ClS(Cl)=O
InChI key
FYSNRJHAOHDILO-UHFFFAOYSA-N
vapor pressure
97 mmHg ( 20 °C)
form
liquid
concentration
2.0 M in methylene chloride
density
1.373 g/mL at 25 °C
Quality Level
signalword
Danger
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3
target_organs
Central nervous system, Respiratory system
supp_hazards
存储类别
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
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)
High-resolution synchrotron far infrared spectroscopy of thionyl chloride: Analysis of the ?3 and ?6 fundamental bands.
Martin-Drumel MA, et al.
Journal of Molecular Spectroscopy (2015)
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
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