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经验公式(希尔记法):
C9H6ClNO2S
化学文摘社编号:
分子量:
227.67
EC Number:
242-515-5
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
156347
MDL number:
Quality Level
assay
≥96.0% (AT)
form
solid
mp
126-129 °C
solubility
methanol: soluble 10 mg/mL, clear, colorless to light yellow
SMILES string
ClS(=O)(=O)c1cccc2cccnc12
InChI
1S/C9H6ClNO2S/c10-14(12,13)8-5-1-3-7-4-2-6-11-9(7)8/h1-6H
InChI key
JUYUYCIJACTHMK-UHFFFAOYSA-N
General description
8-Quinolinesulfonyl chloride reacts with aromatic/heterocyclic sulfonamides containing a free amino, imino, hydrazino or hydroxyl group to form water-soluble compounds.
Application
寡核苷酸合成中的偶联剂;在中等温度下由仲酯形成烯烃
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
H. Takaku et al.
The Journal of Organic Chemistry, 45, 3347-3347 (1980)
H. Takaku et al.
The Journal of Organic Chemistry, 46, 589-589 (1981)
H. Takaku et al.
The Journal of Organic Chemistry, 48, 1399-1399 (1983)
E.J. Corey et al.
The Journal of Organic Chemistry, 54, 389-389 (1989)
Vijay K Agrawal et al.
European journal of medicinal chemistry, 39(7), 593-600 (2004-07-09)
Quantitative structure-activity-relationship (QSAR) study on aromatic/heterocyclic sulfonamides containing 8-quinoline-sulfonyl carbonic anhydrase (CA) inhibitors has been carried out topologically using first-order valence connectivity index ((1)chi(v)). Excellent results are obtained against all the three isozymes; CA I, II and IV of the
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