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Merck
CN

22695

喹啉-8-磺酰氯

≥96.0% (AT)

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关于此项目

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:
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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

pictograms

Corrosion

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

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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