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30-1850

Sigma-Aldrich

Thionyl chloride

SAJ first grade, ≥90.0%

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About This Item

Fórmula linear:
SOCl2
Número CAS:
7719-09-7
Peso molecular:
118.97
Beilstein:
1209273
Número MDL:
MFCD00011449
Código UNSPSC:
12352307
ID de substância PubChem:
329753344

grau

SAJ first grade

pressão de vapor

97 mmHg ( 20 °C)

Ensaio

≥90.0%

forma

liquid

disponibilidade

available only in Japan

índice de refração

n20/D 1.518 (lit.)

pb

79 °C (lit.)

pf

−105 °C (lit.)

densidade

1.631 g/mL at 25 °C (lit.)

temperatura de armazenamento

15-25°C

cadeia de caracteres SMILES

ClS(Cl)=O

InChI

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

chave InChI

FYSNRJHAOHDILO-UHFFFAOYSA-N

Procurando produtos similares? Visita Guia de comparação de produtos

Pictogramas

Skull and crossbonesCorrosion
GHS06,GHS05

Palavra indicadora

Danger

Frases de perigo

H302,H314,H331,H335

Classificações de perigo

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A - STOT SE 3

Órgãos-alvo

Respiratory system

Perigos de suplementos

EUH014,EUH029

Código de classe de armazenamento

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Certificados de análise (COA)

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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
Qingbing Wang et al.
Carbohydrate research, 343(17), 2989-2991 (2008-10-07)
Aldopyranose peracetates react with thionyl chloride and tin tetrachloride, producing the corresponding peracylated aldopyranosyl chlorides in very good to excellent yields (88-100%) with exclusive alpha-anomeric selectivity and short reaction times. The use of peracylated sugars as the substrate in large
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