Di-tert-butyl Disulfide - ≥97%(GC) , CAS No.110-06-5

CAS: 110-06-5 Cat. No.: D154920 Peso molecular: 178.35 Número EC: 203-734-1

GRADE & PURITY ≥97%(GC)

Synonyms

di-t-butyl disulfide | EINECS 203-734-1 | DI-TERT-BUTYLDISULFIDE | RTY9CM6498 | D0225 | Tert-butyl disulfide | NSC-677434 | t-Butyldisulfide | Di-tert-butyl disulfide | Di-tert-butyl disulphide | 2,2,5,5-Tetramethyl-3,4-dithiahexane | BIS(TERT-BUTYL)DISUL

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

Mechanism of the oxidation of di-tert-butyl disulfide in the presence of H2O2 catalyzed by bis(acetylacetonato)oxovanadium and a chiral Schiff-base ligand has been investigated.
Di-tert-butyl disulfide has been used in the preparation of gold-supported thin film from symmetrical and mixed disulphide adsorbates

Specifications

Sinónimos

di-t-butyl disulfide | EINECS 203-734-1 | DI-TERT-BUTYLDISULFIDE | RTY9CM6498 | D0225 | Tert-butyl disulfide | NSC-677434 | t-Butyldisulfide | Di-tert-butyl disulfide | Di-tert-butyl disulphide | 2, 2, 5, 5-Tetramethyl-3, 4-dithiahexane | BIS(TERT-BUTYL)DISUL

Especificaciones y pureza

≥97%(GC)

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥97%(GC)

Nombres e identificadores

• Pubchem Sid: 488183716
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488183716
• Sonrisas canónicas: CC(C)(C)SSC(C)(C)C
• IUPAC Name: 2-(tert-butyldisulfanyl)-2-methylpropane
• InChIKey: BKCNDTDWDGQHSD-UHFFFAOYSA-N
• INCHI: 1S/C8H18S2/c1-7(2,3)9-10-8(4,5)6/h1-6H3
• Isómeros SMILES: CC(C)(C)SSC(C)(C)C
• WGK Alemania: 3
• Peso molecular: 178.35
• Reaxy-Rn: 1698170
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1698170&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organosulfur compounds
    • Clase Organic disulfides
      • Subclass Dialkyldisulfides

• Kingdom: Organic compounds
• Superclass: Organosulfur compounds
• Clase: Organic disulfides
• Subclass: Dialkyldisulfides
• Intermediate Tree Nodes: Not available
• Direct Parent: Dialkyldisulfides
• Alternative Parents: Sulfenyl compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Dialkyldisulfide - Sulfenyl compound - Hydrocarbon derivative - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as dialkyldisulfides. These are organic compounds containing a disulfide group R-SS-R' where R and R' are both alkyl groups.
• 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

Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Air sensitive
• Índice de refracción: n20/D 1.490(lit.)
• Punto de inflamación (°F): 67°C
• Punto de inflamación (°C): 67°C
• Punto de ebullición (°C): 200-201 °C
• Peso molecular: 178.400 g/mol
• XLogP3: 2.900
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 178.085 Da
• Monoisotopic Mass: 178.085 Da
• Topological Polar Surface Area: 50.600 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 80.800
• 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. Jia-Hui Chen, Jia-Hui Lu, Xiao-Lu Pu, Li Chen, Yu-Zhong Wang.  (2022)  Recyclable, malleable and intrinsically flame-retardant epoxy resin with catalytic transesterification.  CHEMOSPHERE,      [PMID:35093421] [10.1016/j.chemosphere.2022.133778]