grade
SAJ first grade
vapor pressure
97 mmHg ( 20 °C)
assay
≥90.0%
form
liquid
availability
available only in Japan
refractive index
n20/D 1.518 (lit.)
bp
79 °C (lit.)
mp
−105 °C (lit.)
density
1.631 g/mL at 25 °C (lit.)
storage temp.
15-25°C
SMILES string
ClS(Cl)=O
InChI
1S/Cl2OS/c1-4(2)3
InChI key
FYSNRJHAOHDILO-UHFFFAOYSA-N
Still not finding the right product?
Explore all of our products under 氯化亚砜
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
法规信息
新产品
此项目有
Xiangshu Xiao et al.
The Journal of organic chemistry, 70(16), 6496-6498 (2005-07-30)
The indeno[1,2-c]isoquinolines are an important class of topoisomerase I inhibitors with anticancer activity. The condensation of Schiff bases with homophthalic anhydrides provides a mixture of cis- and trans-4-carboxy-3,4-dihydro-3-phenyl-1(2H)isoquinolones. Although the cis products can be readily converted to indeno[1,2-c]isoquinolines with thionyl
S Aksoy et al.
Journal of biotechnology, 60(1-2), 37-46 (1998-05-08)
Poly(methyl methacrylate-acrylic acid) microspheres were prepared and the acid groups were activated by using either carbodiimide (CDI) or thionyl chloride (SOCl2). alpha-Amylase was covalently bound on these activated microspheres. The properties of the immobilized enzyme were investigated and compared with
N-9-fluorenylmethoxycarbonylpyroglutamate. Preparation of the acid, chloride and succinimidyl ester.
N L Benoiton et al.
International journal of peptide and protein research, 43(4), 321-324 (1994-04-01)
Fmoc-glutamic acid is converted by thionyl chloride into the dichloride, which spontaneously cyclizes to Fmoc-pyroglutamyl chloride. The latter is stable to water. Pure Fmoc-pyroglutamyl chloride is obtained by washing the reaction mixture with water, which destroys uncyclized dichloride by converting