1-(2-Pyridylazo)-2-naphthol(PAN) - indicator , CAS No.85-85-8

CAS: 85-85-8 Cat. No.: P299392 Peso molecular: 249.27 Número EC: 201-637-9

GRADE & PURITY Indicator

Synonyms

1-(Pyridin-2-azo)-2-naphthol | NCGC00247231-01 | 1-(Pyridin-2-yldiazenyl)naphthalen-2-ol | HMS2310J23 | 1-(2-Pyridylazo)-2-naphthol, for spectrophotometric det. of metal ions, >=97.0% | PAN (indicator) | EINECS 201-637-9 | 095B53Y3XV | (E)-1-(pyridin-2-yl

Storage

Room temperature

Shipped In

Normal

Specifications

Sinónimos

1-(Pyridin-2-azo)-2-naphthol | NCGC00247231-01 | 1-(Pyridin-2-yldiazenyl)naphthalen-2-ol | HMS2310J23 | 1-(2-Pyridylazo)-2-naphthol, for spectrophotometric det. of metal ions, >=97.0% | PAN (indicator) | EINECS 201-637-9 | 095B53Y3XV | (E)-1-(pyridin-2-yl

Especificaciones y pureza

indicator

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Grado

Indicator

Nombres e identificadores

• Pubchem Sid: 504751179
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504751179
• Sonrisas canónicas: C1=CC=C2C(=C1)C=CC(=C2N=NC3=CC=CC=N3)O
• IUPAC Name: 1-(pyridin-2-yldiazenyl)naphthalen-2-ol
• InChIKey: LLYOXZQVOKALCD-UHFFFAOYSA-N
• INCHI: 1S/C15H11N3O/c19-13-9-8-11-5-1-2-6-12(11)15(13)18-17-14-7-3-4-10-16-14/h1-10,19H
• Isómeros SMILES: C1=CC=C2C(=C1)C=CC(=C2N=NC3=CC=CC=N3)O
• WGK Alemania: 3
• Peso molecular: 249.27
• Reaxy-Rn: 206390
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=206390&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Naphthalenes
      • Subclass Naphthols and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Naphthalenes
• Subclass: Naphthols and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Naphthols and derivatives
• Alternative Parents: 1-hydroxy-2-unsubstituted benzenoids Pyridines and derivatives Heteroaromatic compounds Azo compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organooxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: 2-naphthol - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Pyridine - Heteroaromatic compound - Azo compound - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as naphthols and derivatives. These are naphthalene derivatives carrying one or more hydroxyl (-OH) groups at any ring position.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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POLB Tchem DNA polymerase beta (23632 Activities)

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GLB1 Tchem Beta-galactosidase (339 Activities)

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ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

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ALOX12 Tchem Arachidonate 12-lipoxygenase (3262 Activities)

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HSP90AA1 Tchem Heat shock protein HSP 90-alpha (4115 Activities)

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GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)

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PIN1 Tchem Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 (36611 Activities)

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HEK293 (82097 Activities)

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FEN1 Tchem Flap endonuclease 1 (12055 Activities)

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GNAS Tbio Guanine nucleotide-binding protein G(s), subunit alpha (103405 Activities)

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POLH Tchem DNA polymerase eta (21678 Activities)

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KDM4A Tchem Lysine-specific demethylase 4A (52245 Activities)

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EHMT2 Tchem Histone-lysine N-methyltransferase, H3 lysine-9 specific 3 (93046 Activities)

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L3MBTL1 Tchem Lethal(3)malignant brain tumor-like protein 1 (14536 Activities)

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KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)

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NPC1 Tchem Niemann-Pick C1 protein (18985 Activities)

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GMNN Tbio Geminin (128009 Activities)

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MBNL1 Tbio Muscleblind-like protein 1 (34431 Activities)

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CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)

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ATAD5 Tbio ATPase family AAA domain-containing protein 5 (122566 Activities)

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BAZ2B Tchem Bromodomain adjacent to zinc finger domain protein 2B (56204 Activities)

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ATXN2 Tbio Ataxin-2 (54410 Activities)

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IDH1 Tclin Isocitrate dehydrogenase [NADP] cytoplasmic (40980 Activities)

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CGA Tbio Glycoprotein hormones alpha chain (29278 Activities)

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Plasmodium falciparum (966862 Activities)

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INS1 (2867 Activities)

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Rorc Nuclear receptor ROR-gamma (89407 Activities)

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FTL Ferritin light chain (43324 Activities)

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NS1 Nonstructural protein 1 (33327 Activities)

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HSP90 (947 Activities)

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Mecanismos de acción

Propiedades químicas y físicas

• Punto de fusión (°C): 138-141°C
• Peso molecular: 249.270 g/mol
• XLogP3: 3.900
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 249.09 Da
• Monoisotopic Mass: 249.09 Da
• Topological Polar Surface Area: 57.800 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 321.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Lei Jin, Zhao-Yun Wang, Zhuan-Yun Cai, Jia-Qiang Yang, An-Ni Zheng, Fang-Zu Yang, De-Yin Wu, Dongping Zhan.  (2023)  1-(2-Pyridylazo)-2-naphthol as a synergistic additive for improving throwing power of through hole copper electronic electroplating.  JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY,      [PMID:] [10.1016/j.jiec.2023.05.036]

2. Yong Han, Weixia Yang, Xueli Luo, Xie He, Ying Yu, Chunhua Li, Wenzhi Tang, Tianli Yue, Zhonghong Li.  (2019)  Cu2+-Triggered Carbon Dots with Synchronous Response of Dual Emission for Ultrasensitive Ratiometric Fluorescence Determination of Thiophanate-Methyl Residues.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:31618026] [10.1021/acs.jafc.9b04720]

3. Zhonghua Xue, Lulu Xiong, Hao Peng, Honghong Rao, Xiuhui Liu, Xiaoquan Lu.  (2018)  A selective colorimetric sensing strategy for cysteine based on an indicator-displacement mechanism.  NEW JOURNAL OF CHEMISTRY,  42  (6): (4324-4330).  [PMID:] [10.1039/C7NJ03887A]

4. Yang Hu, Lihui Wang, Jie Shen, Guoqiang Jiang, Chengyou Kan.  (2018)  Preparation and characterization of porous cationic poly[styrene-co-(N,N′-dimethylaminoethyl methacrylate)] nanoparticles and their adsorption of heavy metal ions in water.  POLYMER INTERNATIONAL,  67  (5): (535-543).  [PMID:] [10.1002/pi.5541]

5. Fan Chunlei, Pan Qinhe, Li Qun, Wang Liyuan.  (2015)  Cloud point-TiO2/sepiolite composites extraction for simultaneous preconcentration and determination of nickel in green tea and coconut water.  Journal of the Iranian Chemical Society,  13  (2): (331-337).  [PMID:] [10.1007/s13738-015-0741-6]

6. Iqbal Jibran, Yin Changhai, Geng Jinpei, Li Xiaoyu, Li Xiuyong, Du Yiping, Liu Bing Xiang.  (2012)  Ultra-sensitive spectrophotometric determination of nickel after complexation and membrane filtration.  MICROCHIMICA ACTA,  177  (1): (195-200).  [PMID:] [10.1007/s00604-012-0778-5]

7. Sangsang Liu, Qin Yu, Haitao Liu, Wenlong Chen, Fugang Qi, Yilong Dai, Yaru Liang, Weihong Lai, Xiaoping Ouyang.  (2024)  A multifunctional protective layer filled with 2D anionic nanosheets enabling a dendrite-free zinc anode.  Inorganic Chemistry Frontiers,  11  (4): (1135-1144).  [PMID:] [10.1039/D3QI01981K]

8. Wanting Ma, Shengchao Xu, Qifeng Wei, Xiulian Ren.  (2024)  Density, acidity and theoretical calculation of hydrophobic deep eutectic solvents formed by amide and lactic acid.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2024.125547]