371491
氯化亚砜
technical grade
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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
EC Number:
231-748-8
UNSPSC Code:
12352300
PubChem Substance ID:
Beilstein/REAXYS Number:
1209273
MDL number:
Grade:
technical grade
Form:
liquid
InChI key
FYSNRJHAOHDILO-UHFFFAOYSA-N
InChI
1S/Cl2OS/c1-4(2)3
SMILES string
ClS(Cl)=O
grade
technical grade
vapor pressure
97 mmHg ( 20 °C)
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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signalword
Danger
hcodes
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
新产品
此项目有
Tom Godau et al.
Dalton transactions (Cambridge, England : 2003), 40(24), 6547-6554 (2011-05-18)
One-pot syntheses of three new enantiopure heteroscorpionate ligands derived from (+)-camphor or (-)-menthone are described. The ligands are obtained by reacting pyrazoles derived from (+)-camphor or (-)-menthone with sodium hydride and thionyl chloride. Subsequent reactions with pyridine and various aldehydes
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
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.
Reaction of some 1,2-trans-aldose peracetates with thionyl chloride-acetic acid--a convenient synthesis of some 1,2-trans-per-O-acetyl-D-glycosyl chlorides.
G J Chittenden
Carbohydrate research, 242, 297-301 (1993-04-07)
Roberta Cassano et al.
Biomacromolecules, 11(7), 1716-1720 (2010-06-12)
In the present work, we report on the synthesis of cellulose cotton fibers covalently linked to diclofenac moieties and the evaluation of the anti-inflammatory activity of this new biomaterial. In spite of recent progress in experimental and clinical medicine, the
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