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Merck
CN

33626

Sigma-Aldrich

对氨基苯磺酰胺

puriss. p.a., ≥98% (calc. to the dried substance)

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别名:
对氨基苯磺酰胺
线性分子式:
H2NC6H4SO2NH2
CAS号:
分子量:
172.20
Beilstein:
511852
EC 号:
MDL编号:
UNSPSC代码:
12352100
eCl@ss:
39093202
PubChem化学物质编号:
NACRES:
NA.21

等级

puriss. p.a.

质量水平

检测方案

≥98% (calc. to the dried substance)

形式

solid

杂质

≤0.002% heavy metals (as Pb)

灼烧残渣

≤0.1% (as SO4)

缺失

≤0.5% loss on drying, 105 °C

颜色

white to faint beige

mp

163-166 °C
164-166 °C (lit.)

痕量阴离子

chloride (Cl-): ≤100 mg/kg
sulfate (SO42-): ≤200 mg/kg

抗生素抗菌谱

Gram-negative bacteria
Gram-positive bacteria

作用机制

DNA synthesis | interferes
enzyme | inhibits

SMILES字符串

Nc1ccc(cc1)S(N)(=O)=O

InChI

1S/C6H8N2O2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,7H2,(H2,8,9,10)

InChI key

FDDDEECHVMSUSB-UHFFFAOYSA-N

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一般描述

化学结构:磺胺
磺胺(氨基苯磺酰胺)是一种氨基取代的苯磺酰胺。其-单和二碘衍生物已被合成。

应用

  • Study of new azo-azomethine derivatives of sulfanilamide: synthesis, characterization, spectroscopic, antimicrobial, antioxidant and anticancer activity: This study explores new derivatives of sulfanilamide synthesized through diazonium salt reactions and coupling with 2-hydroxy-3-methoxybenzaldehyde, providing insights into their potential antimicrobial, antioxidant, and anticancer activities (HS Al-Atbi, IJ Al-Assadi, et al., 2020).

包装

33626-100G; 33626-6X100G

其他说明

保存于密闭容器内,置于干燥通风处。

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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Traci L Ness et al.
Journal of immunology (Baltimore, Md. : 1950), 173(11), 6938-6948 (2004-11-24)
CCR1 has previously been shown to play important roles in leukocyte trafficking, pathogen clearance, and the type 1/type 2 cytokine balance, although very little is known about its role in the host response during sepsis. In a cecal ligation and
Caroline A Dobbin et al.
Journal of immunology (Baltimore, Md. : 1950), 169(2), 958-965 (2002-07-05)
We propose that the 70-kDa heat shock protein (HSP70) protects virulent Toxoplasma gondii from the effects of the host by immunomodulation. This hypothesis was tested using quercetin and antisense oligonucleotides targeting the start codon of the virulent T. gondii HSP70
Joseph A Hollenbaugh et al.
Journal of immunology (Baltimore, Md. : 1950), 177(5), 3004-3011 (2006-08-22)
We previously reported that IFN-gamma secreted by donor cytotoxic T cell 1 (Tc1) cells was the most important factor in promoting EG7 (an OVA transfection the EL4 thymoma) rejection in mice. In this study, we show that the ability of
The Iodination of p-Aminobenzenesulfonamide and Some Symmetrical Azobenzenesulfonamides.
Scudi JV.
Journal of the American Chemical Society, 59(8), 1480-1483 (1937)
Edward E Knaus et al.
Bioorganic & medicinal chemistry letters, 21(19), 5892-5896 (2011-08-20)
A series of compounds incorporating regioisomeric phenylethynylbenzenesulfonamide moieties has been investigated for the inhibition of four human carbonic anhydrase (hCA, EC 4.2.1.1) isoforms, hCA I, II, IX and XII. Inhibition between the low nanomolar to the milliomolar range has been

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