Cartap hydrochloride - ≥97% , CAS No.15263-52-2

CAS: 15263-52-2 Cat. No.: C1434133 Peso molecular: 273.8 Beilstein Registry Number: 5157539 Número EC: 239-309-2 PubChem CID: 30913

GRADE & PURITY ≥97%

Storage

Room temperature,Cool

Shipped In

Normal

Descripción general

Cartap hydrochloride, an organonitrogen insecticide, can cause a marked irreversible Ca 2+ -dependent contracture in both isolated mouse and rabbit phrenic nerve-diaphragms. Cartap hydrochloride significantly increases the level of endogenous reactive oxygen species (ROS) in C2C12 cells.

Specifications

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Room temperature, Cool

Enviado en

Normal

Pureza

≥97%

Nombres e identificadores

• Sonrisas canónicas: CN(C)C(CSC(=O)N)CSC(=O)N.Cl
• IUPAC Name: S-[3-carbamoylsulfanyl-2-(dimethylamino)propyl] carbamothioate;hydrochloride
• InChIKey: MSHXTAQSSIEBQS-UHFFFAOYSA-N
• INCHI: 1S/C7H15N3O2S2.ClH/c1-10(2)5(3-13-6(8)11)4-14-7(9)12;/h5H,3-4H2,1-2H3,(H2,8,11)(H2,9,12);1H
• Isómeros SMILES: CN(C)C(CSC(=O)N)CSC(=O)N.Cl
• WGK Alemania: 3
• RTECS: FD1225000
• PubChem CID: 30913
• Peso molecular: 273.8
• Beilstein: 5157539

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organosulfur compounds
    • Clase Thiocarbonyl compounds
      • Subclass Thiocarbamic acid derivatives

• Kingdom: Organic compounds
• Superclass: Organosulfur compounds
• Clase: Thiocarbonyl compounds
• Subclass: Thiocarbamic acid derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Thiocarbamic acid derivatives
• Alternative Parents: Trialkylamines Organic carbonic acids and derivatives Sulfenyl compounds Organopnictogen compounds Organic zwitterions Organic oxides Organic chloride salts Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Carbonic acid derivative - Tertiary amine - Thiocarbamic acid derivative - Tertiary aliphatic amine - Sulfenyl compound - Amine - Organic chloride salt - Organic salt - Organic zwitterion - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as thiocarbamic acid derivatives. These are organic compounds containing a functional group with the general structure OC(=S)NR2 or SC(=O)NR2.
• 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

Referencias

1. Chen Yunhai, Zhu Xuecheng, Liu Huilin, Sun Baoguo.  (2024)  Multi-confinement structured carbon dots with long room temperature phosphorescence lifetime and efficiency for sensing thiram residues assisted by copper ions.  MICROCHIMICA ACTA,  191  (11): (1-11).  [PMID:39379669] [10.1007/s00604-024-06732-3]

2. Yunhai Chen, Xuecheng Zhu, Huilin Liu, Baoguo Sun.  (2025)  Confining monochromophore in polymer network for fluorescence-phosphorescence dual-emission sensing of thiram.  FOOD CHEMISTRY,      [PMID:40784161] [10.1016/j.foodchem.2025.145825]

3. Chen Yunhai, Zhu Xuecheng, Liu Huilin, Sun Baoguo.  (2025)  Synergistic PET/IFE-driven fluorescence-phosphorescence dual signal quenching in RTP CDs sensor for sensitive thiram monitoring in food safety.  MICROCHIMICA ACTA,  192  (7): (1-10).  [PMID:40506556] [10.1007/s00604-025-07291-x]