2,3-Dichlorophenylhydrazine Hydrochloride - ≥97% , CAS No.21938-47-6

CAS: 21938-47-6 Cat. No.: D132563 Summenformel: C₆H₆Cl₂N₂·HCl Molekulargewicht: 213.49 EG-Nummer: 630-710-1

GRADE & PURITY ≥97%

Synonyms

(2,3-Dichlorophenyl)hydrazinehydrochloride | RHNATWVYOKUFLK-UHFFFAOYSA-N | FT-0609578 | (2,3-Dichloro-phenyl)-hydrazine hydrogen chloride | EN300-251592 | 2,3-Dichloro phenylhydrazine Hydrochloride | D2641 | SB79375 | Hydrazine, (2,3-dichlorophenyl)-, mon

Storage

Room temperature

Shipped In

Normal

Specifications

Synonyme

(2,3-Dichlorophenyl)hydrazinehydrochloride | RHNATWVYOKUFLK-UHFFFAOYSA-N | FT-0609578 | (2,3-Dichloro-phenyl)-hydrazine hydrogen chloride | EN300-251592 | 2,3-Dichloro phenylhydrazine Hydrochloride | D2641 | SB79375 | Hydrazine, (2,3-dichlorophenyl)-, mon

Spezifikationen & Reinheit

≥97%

Storage

Room temperature

Verschickt in

Normal

Reinheit

≥97%

Namen und Kennungen

• Pubchem Sid: 488198000
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488198000
• Kanonisches Lächeln: C1=CC(=C(C(=C1)Cl)Cl)NN.Cl
• IUPAC Name: (2,3-dichlorophenyl)hydrazine;hydrochloride
• InChIKey: RHNATWVYOKUFLK-UHFFFAOYSA-N
• INCHI: 1S/C6H6Cl2N2.ClH/c7-4-2-1-3-5(10-9)6(4)8;/h1-3,10H,9H2;1H
• Isomere SMILES: C1=CC(=C(C(=C1)Cl)Cl)NN.Cl
• Alternative CAS-Nummer: 13147-14-3
• Molekulargewicht: 213.49
• Reaxy-Rn: 3708910
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3708910&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Klasse Benzene and substituted derivatives
      • Subclass Halobenzenes
        • Ebene5 Chlorobenzenes
          • Ebene6 Dichlorobenzenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: Benzene and substituted derivatives
• Subclass: Halobenzenes
• Intermediate Tree Nodes: Chlorobenzenes
• Direct Parent: Dichlorobenzenes
• Alternative Parents: Phenylhydrazines Aryl chlorides Organopnictogen compounds Organonitrogen compounds Organochlorides Organic zwitterions Organic chloride salts Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenylhydrazine - 1,2-dichlorobenzene - Aryl halide - Aryl chloride - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organic chloride salt - Organic salt - Organic zwitterion - Organonitrogen compound - Organochloride - Organohalogen compound - Aromatic homomonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as dichlorobenzenes. These are compounds containing a benzene with exactly two chlorine atoms attached to it.
• 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

Chemische und physikalische Eigenschaften

• Empfindlichkeit: Air Sensitive,Hygroscopic
• Molekulargewicht: 213.500 g/mol
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 211.967 Da
• Monoisotopic Mass: 211.967 Da
• Topological Polar Surface Area: 38.100 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 110.000
• 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: 2

XLogP3

Referenzen

1. Chunling Ren, Xiao Xu, Dan Yan, Mengzhen Gu, Jinghan Zhang, Haili Zhang, Chao Han, Lingyi Kong.  (2022)  Dual-action nanoplatform with a synergetic strategy to promote oxygen accumulation for enhanced photodynamic therapy against hypoxic tumors.  Acta Biomaterialia,      [PMID:35526738] [10.1016/j.actbio.2022.04.035]

2. Dan Chen, Ya-Xian Wu, Yu-bao Qiu, Bin-bin Wan, Gang Liu, Jun-liang Chen, Mu-dan Lu, Qing-feng Pang.  (2019)  Hyperoside suppresses hypoxia-induced A549 survival and proliferation through ferrous accumulation via AMPK/HO-1 axis.  PHYTOMEDICINE,      [PMID:31881478] [10.1016/j.phymed.2019.153138]