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308560

4-氨基-6-氯-1,3-苯二磺酰胺

Name: 4-氨基-6-氯-1,3-苯二磺酰胺
Brand: ALDRICH

98%

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别名:

5-氯-2,4-二磺酰胺基苯胺, 4-氨基-6-氯-1,3-苯二磺酰胺

线性分子式:

H₂NC₆H₂(Cl)(SO₂NH₂)₂

CAS号:

121-30-2

分子量:

285.73

Beilstein:

1083877

EC 号:

204-463-1

MDL编号:

MFCD00007933

PubChem化学物质编号:

24858677

NACRES:

NA.22

检测方案

98%

形式

powder

mp

257-261 °C (lit.)

SMILES字符串

Nc1cc(Cl)c(cc1S(N)(=O)=O)S(N)(=O)=O

InChI

1S/C6H8ClN3O4S2/c7-3-1-4(8)6(16(10,13)14)2-5(3)15(9,11)12/h1-2H,8H2,(H2,9,11,12)(H2,10,13,14)

InChI key

IHJCXVZDYSXXFT-UHFFFAOYSA-N

基因信息

human ... CA1(759) , CA2(760) , CA5A(763) , CA5B(11238) , CA9(768)

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一般描述

4-氨基-6-氯-1,3-苯二磺酰胺是胃病原体幽门螺杆菌（Helicobacter pylori ，hpCA）的有效抑制剂。

应用

4-氨基-6-氯-1,3-苯二磺酰胺通过与适当标记的醛缩合，可用于合成氘代噻嗪类化合物。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

分析证书(COA)

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示例

T1503

货号

25G

包装规格/数量

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705578-5MG-PW

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MMYOMAG-74K-13

1000309185

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Mass spectrometric behavior of thiazide-based diuretics after electrospray ionization and collision-induced dissociation.

Mario Thevis et al.

Analytical chemistry, 74(15), 3802-3808 (2002-08-15)

The mass spectrometric behavior of 21 thiazide-based compounds after electrospray ionization in the negative ion mode and collision-induced dissociation was investigated on a triple-stage quadrupole mass spectrometer. The mass spectra show individual and common fragmentation patterns, the generations of which

Validated micellar electrokinetic capillary chromatography method for quality control of the drug substances hydrochlorothiazide and chlorothiazide.

B R Thomas et al.

Journal of chromatography. B, Biomedical applications, 657(2), 383-394 (1994-07-15)

A stability-indicating, quality control analysis method was developed and validated for the diuretic drug substances hydrochlorothiazide (HCTZ) and chlorothiazide (CTZ). Micellar electrokinetic capillary chromatography employing the anionic detergent sodium dodecyl sulfate at 30 mM in 20 mM sodium borate buffer

Binding of 2-amino-4-chloro-m-benzenedisulfonamide as a metabolite of hydrochlorothiazide to erythrocytes.

M Yamazaki et al.

Chemical & pharmaceutical bulletin, 38(10), 2882-2883 (1990-10-01)

2-Amino-4-chloro-m-benzenedisulfonamide (ACBS) is a metabolite of hydrochlorothiazide. We reported that the ACBS concentration in erythrocytes was higher than in plasma in a patient. Therefore the binding of ACBS to rabbit erythrocyte was studied. The Scatchard plot showed the nonlinear plot

Biopharmaceutical studies of thiazide diuretics. III. In vivo formation of 2-amino-4-chloro-m-benzenedisulfonamide as a metabolite of hydrochlorothiazide in a patient.

T Okuda et al.

Chemical & pharmaceutical bulletin, 35(8), 3516-3518 (1987-08-01)

Detection of urinary markers for thiazide diuretics after oral administration of hydrochlorothiazide and altizide-relevance to doping control analysis.

K Deventer et al.

Journal of chromatography. A, 1216(12), 2466-2473 (2009-02-04)

In sports, thiazide diuretics are used to flush out previously taken prohibited substances with forced diuresis and in sports where weight classes are involved to achieve acute weight loss. Thiazide diuretics include compounds which are very unstable and hydrolyse in

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