Cas no 1843-21-6 (N-Phenyl-1,3-benzothiazol-2-amine)

N-Phenyl-1,3-benzothiazol-2-amine structure
1843-21-6 structure
Product Name:N-Phenyl-1,3-benzothiazol-2-amine
CAS No:1843-21-6
MF:C13H10N2S
MW:226.296901226044
MDL:MFCD00453249
CID:173512
PubChem ID:230981
Update Time:2025-04-24

N-Phenyl-1,3-benzothiazol-2-amine Chemical and Physical Properties

Names and Identifiers

    • 2-Benzothiazolamine,N-phenyl-
    • Benzothiazol-2-yl-phenyl-amine
    • N-phenyl-1,3-benzothiazol-2-amine
    • 2-anilinobenzothiazole
    • 2-phenylaminobenzothiazole
    • 4-benzothiazol-2-yl-phenylamine
    • AC1L5KP7
    • AC1Q4TO3
    • AC1Q4WFW
    • Benzothiazole, 2-anilino-
    • benzothiazolyl-phenyl-amine
    • N-phenyl-2-benzothiazolamine
    • N-phenyl-2-benzothiazolylamine
    • N-phenylbenzo[d]thiazol-2-amine
    • N-phenylbenzothiazol-2-amine
    • NSC26434
    • N-Phenylbenzothiazole-2-amine
    • 1,3-benzothiazol-2-yl(phenyl)amine
    • 2-phenyliminobenzothiazole
    • MLS001007555
    • NSC-26434
    • 2-Benzothiazolamine, N-phenyl-
    • NS00124628
    • N-(1,3-BENZOTHIAZOL-2-YL)-N-PHENYLAMINE
    • AKOS001074996
    • Anilinobenzothiazole
    • CHEMBL1338489
    • VS-01425
    • CS-0232745
    • EN300-12846
    • InChI=1/C13H10N2S/c1-2-6-10(7-3-1)14-13-15-11-8-4-5-9-12(11)16-13/h1-9H,(H,14,15
    • Benzothiazol-2-amine, N-phenyl-
    • DTXSID6047735
    • HMS2666J07
    • BB 0218612
    • MFCD00453249
    • cid_230981
    • SMR000384688
    • 1843-21-6
    • BAA84321
    • HMS1748F07
    • BDBM76561
    • N-Phenyl-1,3-benzothiazol-2-amine #
    • K2SX7MY84E
    • SY008042
    • Z85923142
    • E75904
    • SCHEMBL1821021
    • STK042950
    • DS-012986
    • BBL003825
    • N-Phenyl-1,3-benzothiazol-2-amine
    • MDL: MFCD00453249
    • Inchi: 1S/C13H10N2S/c1-2-6-10(7-3-1)14-13-15-11-8-4-5-9-12(11)16-13/h1-9H,(H,14,15)
    • InChI Key: QDTDFSFRIDFTCF-UHFFFAOYSA-N
    • SMILES: S1C(=NC2C=CC=CC1=2)NC1C=CC=CC=1

Computed Properties

  • Exact Mass: 226.0566
  • Monoisotopic Mass: 226.05646950g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 1
  • Complexity: 228
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 4.1
  • Topological Polar Surface Area: 53.2?2

Experimental Properties

  • Density: 1.3±0.1 g/cm3
  • Melting Point: 139-141 °C
  • Boiling Point: 374.5±25.0 °C at 760 mmHg
  • Flash Point: 180.3±23.2 °C
  • PSA: 24.92
  • LogP: 4.11290
  • Vapor Pressure: 0.0±0.8 mmHg at 25°C

N-Phenyl-1,3-benzothiazol-2-amine Security Information

N-Phenyl-1,3-benzothiazol-2-amine Pricemore >>

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N-Phenyl-1,3-benzothiazol-2-amine Related Literature

Additional information on N-Phenyl-1,3-benzothiazol-2-amine

Comprehensive Overview of 2-Benzothiazolamine,N-phenyl- (CAS No. 1843-21-6)

2-Benzothiazolamine,N-phenyl- (CAS No. 1843-21-6) is a specialized organic compound that belongs to the benzothiazole family. This compound is widely recognized for its unique chemical properties and diverse applications in various industries. The molecular structure of N-phenyl-2-benzothiazolamine features a benzothiazole core with an amine group and a phenyl substituent, which contributes to its distinct reactivity and functionality. Researchers and industry professionals often seek information on this compound due to its relevance in advanced material science and specialty chemical formulations.

The benzothiazole derivatives, including 2-Benzothiazolamine,N-phenyl-, have garnered significant attention in recent years due to their potential in high-performance applications. One of the most frequently searched questions related to this compound is: "What are the industrial uses of N-phenyl-2-benzothiazolamine?" This reflects the growing interest in its practical applications. The compound is commonly utilized as an intermediate in the synthesis of dyes, pigments, and functional materials. Its ability to act as a ligand or a building block in coordination chemistry makes it valuable for developing novel catalysts and polymers.

Another trending topic in the context of 2-Benzothiazolamine,N-phenyl- is its role in green chemistry and sustainable processes. With increasing environmental regulations, industries are exploring eco-friendly alternatives, and this compound has shown promise due to its moderate toxicity profile and biodegradability. Researchers are investigating its use in water treatment formulations and as a corrosion inhibitor, addressing common queries like "Is N-phenyl-2-benzothiazolamine environmentally friendly?" These studies align with the global shift toward sustainable chemical solutions.

The synthesis and characterization of CAS 1843-21-6 are also subjects of scientific interest. Advanced techniques such as nuclear magnetic resonance (NMR) spectroscopy and high-performance liquid chromatography (HPLC) are employed to ensure the purity and quality of the compound. Analytical data and spectral properties of N-phenyl-2-benzothiazolamine are often requested by chemists and quality control professionals, highlighting the need for accurate and detailed technical information.

In the pharmaceutical sector, benzothiazole-based compounds like 2-Benzothiazolamine,N-phenyl- are being studied for their bioactive potential. While this specific compound is not a drug, its structural motif is present in several pharmacologically active molecules. This connection has led to searches such as "Can N-phenyl-2-benzothiazolamine be used in drug development?" Although direct medicinal applications are limited, its derivatives are explored for antimicrobial and anti-inflammatory properties.

The market dynamics of 2-Benzothiazolamine,N-phenyl- are influenced by its demand in niche applications. Suppliers and manufacturers often highlight its availability in various purity grades, catering to research laboratories and industrial users. Pricing trends and supply chain stability are critical factors for buyers, as reflected in searches like "Where to buy high-purity N-phenyl-2-benzothiazolamine?" The compound's niche status ensures consistent demand from specialized sectors.

Safety and handling guidelines for CAS 1843-21-6 are another area of frequent inquiry. Proper storage conditions, personal protective equipment (PPE) recommendations, and disposal methods are essential for safe laboratory practices. Users often search for "MSDS of 2-Benzothiazolamine,N-phenyl-" to access detailed safety data. While the compound is not classified as highly hazardous, standard precautions for handling organic chemicals should always be followed.

In summary, 2-Benzothiazolamine,N-phenyl- (CAS No. 1843-21-6) is a versatile compound with significant industrial and research relevance. Its applications span from material science to environmental chemistry, making it a subject of ongoing interest. By addressing common questions and aligning with current trends like sustainability and advanced materials, this overview provides valuable insights for professionals and researchers seeking in-depth knowledge about this benzothiazole derivative.

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