4-Amino-6-Chloro-1,3-Benzendisulfonamide 4-氨基-6-氯-1,3-苯二磺酰胺

CAS 121-30-2 MFCD00007933

化学结构图

121-30-2
SMILES: Nc1cc(Cl)c(S(N)(=O)=O)cc1S(N)(=O)=O

化学属性

Mol. FormulaC6H8ClN3O4S2
Mol. Weight286
Melting Point257-261
Appearance 结晶。熔点251-252℃(257-261℃)。略溶于水。

别名和识别编码

Chemical Name4-Amino-6-Chloro-1,3-Benzendisulfonamide
CAS Number121-30-2
Alfabeta NameAMINOCHLOROBENZENEDISULFONAMIDE 4613-----,
MDL NumberMFCD00007933
Synonym 1,3-Benzenedisulfonamide, 4-amino-6-chloro- 1-AMINO-3-CHLORO-4,6-BENZENE- DISULFONAMIDE 3-Chloro-4,6-disulfamoylaniline; 5-Chloro-2,4-disulfamoylaniline 3-chloroaniline-4,6-disulfonamide 3-​Chloroaniline-​4,6-​disulfonamide, 4-​Amino-​6-​chlorobenzene-​1,3-​disulfonamide 4-AMINO-6-CHLORO-1,3-BENZENEDISULFONAMIDE 4-AMINO-6-CHLORO-1,3-BENZENEDISULFONAMIDE 99+% 4-AMINO-6-CHLOROBENZENE-1,3-DISULFONAMIDE 4-amino-6-chloro-3-benzenedisulfonamide 4-氨基-6-氯-1,3-苯二磺酰胺 5-氯-2,4-二磺酰胺基苯胺 4-氨基-6-氯-1,3-苯二磺酰胺 Benzothiadiazine realted compound A 5-CHLORO-2,4-BIS(SULFONAMIDE)ANILINE 5-Chloro-2,4-bis(sulfonamido)aniline 5-氯-2,4-二氨磺酰胺苯胺 Chloruminophenamide NSC 93772 Salamide
PubChem Substance ID87562817
Beilstein Registry Number1083877
EC Number204-463-1
Reaxys-RN1083877
Merck Number2076
Chemical Name Translation4-氨基-6-氯-1,3-苯二磺酰胺
LabNetwork Molecule IDLN00159741
InChIInChI=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)
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分类

  • {SNA} Analytical Standards, Analytical/Chromatography, Chromatography, Hydrochlorothiazide Impurities, Pharmaceutical Impurities, Pharmaceutical Secondary Standards, Pharmaceutical Standards
  • {SNA} Analytical Standards, Analytical/Chromatography, Chromatography, Pharmaceutical Standards, Pharmacopeia Standards, USP Standards, USP Standards A - B
  • {SNA} Additional Standards, Analytical Standards, Chromatography, Hydrochlorothiazide Impurities, Pharmaceutical Impurities, Pharmaceutical Secondary Standards, Pharmaceutical Standards, 分析/色谱
  • {SNA} Building Blocks
  • Sulfur & Selenium Compounds
  • {SNA} Building Blocks, Chemical Synthesis,

产品应用

  • Diuretic.

相关文献及参考

  • Fliri, A., et al.: J. Med. Chem., 52, 8038 (2009),
  • Joshi, S., et al.: J. Pharm. Biomed. Anal., 52, 362 (2010),
  • Castillo-Garit, J., et al.: Eur. J. Pharm. Sci., 39, 30 (2010),

安全信息

Warnings IRRITANT
WGK Germany3
Personal Protective Equipment Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Hazard Codes T
Safety Statements
  • S22 Do not breathe dust 不要吸入粉尘;
  • S26 In case of contact with eyes, rinse immediately with plenty of water and seek medical advice 眼睛接触后,立即用大量水冲洗并征求医生意见;
  • S28 After contact with skin, wash immediately with plenty of ... (to be specified by the manufacturer) 皮肤接触后,立即用大量…(由生产厂家指定)冲洗;
  • S36/37 Wear suitable protective clothing and gloves 穿戴适当的防护服和手套;
  • S36/37/39 Wear suitable protective clothing, gloves and eye/face protection 穿戴适当的防护服、手套和眼睛/面保护;
Risk Statements
  • R20/21 Harmful by inhalation and in contact with skin 吸入及与皮肤接触有害
  • R23/24 Toxic by inhalation and in contact with skin 吸入及皮肤接触都有毒
  • R33 Danger of cumulative effects 有累积作用的危险
Signal word Warning
Hazard statements
  • H315 Causes skin irritation 会刺激皮肤
Precautionary statements
  • P264 Wash hands thoroughly after handling. 处理后要彻底洗净双手。
  • P280 Wear protective gloves/protective clothing/eye protection/face protection. 戴防护手套/防护服/眼睛的保护物/面部保护物。
  • P302+P350
  • P302+P352+P332+P313+P362+P364
  • P305+P351+P338+P337+P313
  • P332+P313
  • P362 Take off contaminated clothing and wash before reuse. 脱掉污染的衣服,清洗后方可重新使用
GHS Symbol

其他信息

  • 图谱信息:5-氯-2,4-二磺酰胺基苯胺(121-30-2)红外图谱(IR1) 5-氯-2,4-二磺酰胺基苯胺(121-30-2)红外图谱(IR2) 5-氯-2,4-二磺酰胺基苯胺(121-30-2)核磁图( 13 CNMR)
  • MSDS 信息:3-Chloro-4,6-disulfamoylaniline(121-30-2).msds
  • TCI Shanghai:4-氨基-6-氯-1,3-苯二磺酰胺 4-Amino-6-chloro-1,3-benzenedisulfonamide,>;98.0%(T)(121-30-2)
  • 用途二:药物双氢氯噻嗪的中间体。
  • Sigma Aldrich:121-30-2(sigmaaldrich)
  • 上游原料:3-氯苯胺 --> 氯胺 T
  • 5-氯-2,4-二磺酰胺基苯胺价格(试剂级):更新日期 产品编号 产品名称 包装 价格 2014/06/02 A1362 4-氨基-6-氯-1,3-苯二磺酰胺 4-Amino-6-chloro-1,3-benzenedisulfonamide 25G 310元
  • 用途一:用作医药中间体,可用于合成氢氯噻嗪等原料药
  • MOL 文件:121-30-2.mol
  • 方法一:间氯苯胺经氯磺酸氯磺化、液氯胺化而得。

系列性分类


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