2-氨基-5-硝基苯磺酸 | 96-75-3
中文名称:
2-氨基-5-硝基苯磺酸
英文名称:
2-Amino-5-nitrobenzenesulfonic acid
CAS No.:
96-75-3
分子式:
C6 H6 N2 O5 S
分子量:
218.187240123749
名称和标识符
MDL
MFCD00035755
InChIKey
LTASFWDWBYFZQQ-UHFFFAOYSA-N
Inchi
1S/C6H6N2O5S/c7-5-2-1-4(8(9)10)3-6(5)14(11,12)13/h1-3H,7H2,(H,11,12,13)
SMILES
[O-][N+](C1C=C(S(O)(=O)=O)C(N)=CC=1)=O
BRN
2654142
别名信息
- 中文别名 -
2-氨基-5-硝基苯磺酸
对硝基苯胺邻磺酸
对硝基苯胺-2-磺酸
- 英文别名 -
2-Amino-5-nitrobenzenesulfonic acid
4-Nitroaniline-2-sulfonic acid
Para Nitro Aniline-2-Sulfonic Acid
P-NITRO ANILINE-O-SULFONIC ACID
4-NITRO-2-SULFOANILINE
2-amino-5-nitrobenzenesulphonic acid
3-AMINO-2-FLUORO-4-PICOLINE
BENZENESULFONIC ACID,2-AMINO-5-NITRO-
P-NITROANILINE-2-SULPHONICACID
P-NITROANLINE-2-SULPHONIC ACID
p-Nitroaniline-o-sulfonic acid
Benzenesulfonic acid, 2-amino-5-nitro-
p-Nitroaniline-2-sulfonic acid
2-amino-5-nitro-benzenesulfonic acid
p-nitroanilin-o-sulphonic acid
p-nitroaniline-o-sulphonic acid
AK114008
P-Nitroaniline-2-Sulphonic acid
NSC7540
PubChem21798
WLN: WSQR BZ ENW
2-Amino-5-nitrobenzenesulfonic acid (ACI)
1-Amino-4-nitrobenzene-2-sulfonic acid
2-Amino-5-nitrobenzene-1-sulfonic acid
4-Nitro-2-sulfoaniline
5-Nitro-2-aminobenzenesulfonic acid
NSC 7540
物化性质
实验特性
LogP
2.60890
PSA
134.59000
折射率
1.6490 (estimate)
密度
1.559 (estimate)
计算特性
精确分子量
218.00000
氢键供体数量
2
氢键受体数量
6
可旋转化学键数量
1
重原子数量
14
复杂度
316
同位素原子数量
0
确定原子立构中心数量
0
不确定原子立构中心数量
0
确定化学键立构中心数量
0
不确定化学键立构中心数量
0
共价键单元数量
1
疏水参数计算参考值(XlogP)
0.4
互变异构体数量
无
表面电荷
0
拓扑分子极性表面积
135
海关数据
海关编码
2921420090
海关数据
中国海关编码:
2921420090
概述:
2921420090 其他苯胺衍生物及其盐. 增值税率:17.0% 退税率:9.0% 监管条件:无 最惠国关税:6.5% 普通关税:30.0%
申报要素:
品名, 成分含量, 用途
Summary:
HS:2921420090 aniline derivatives and their salts VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%
相关文献
1.
A facile single crystal to single crystal transition with significant structural contraction on desolvation
Jane V. Knichal,William J. Gee,Andrew D. Burrows,Paul R. Raithby,Simon J. Teat,Chick C. Wilson Chem. Commun. 2014 50 14436
2.
NI(ii) phosphine and phosphide complexes supported by a PNP-pyrrole pincer ligand
Julie A. Kessler,Vlad M. Iluc Dalton Trans. 2017 46 12125
3.
NI(ii) phosphine and phosphide complexes supported by a PNP-pyrrole pincer ligand
Julie A. Kessler,Vlad M. Iluc Dalton Trans. 2017 46 12125
4.
A straightforward and generalizable synthetic methodology for the synthesis of ruthenium(ii) complexes with thioether ligands from either Ru(iii) or Ru(0) precursors
Biplab K. Maiti,Helmar G?rls,Olaf Klobes,Wolfgang Imhof Dalton Trans. 2010 39 5713
5.
Electrokinetic behaviour of carborundum
A. J. Ham,W. Hodgson Trans. Faraday Soc. 1942 38 217
6.
Reactivity in nucleophilic substitution. Part IV. A carbonyl elimination reaction of 9-fluorenyl toluene-p-sulphonate
G. W. Cowell,A. Ledwith,D. G. Morris J. Chem. Soc. B 1967 697
7.
Reactivity in nucleophilic substitution. Part IV. A carbonyl elimination reaction of 9-fluorenyl toluene-p-sulphonate
G. W. Cowell,A. Ledwith,D. G. Morris J. Chem. Soc. B 1967 697
8.
Calix[4]arene-5,17-dicarboxylic acids and their interactions with aliphatic amines. Part 2. A crystal engineering approach
Frederik C. Krebs,Mikkel J?rgensen J. Chem. Soc. Perkin Trans. 2 2000 1935
9.
CLXVII.—Researches on the freezing points of binary mixtures of organic substances: the behaviour of the dihydric phenols towards p-toluidine, α-naphthylamine, and picric acid
James Charles Philip,Sydney Herbert Smith J. Chem. Soc. Trans. 1905 87 1735
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