Dibenzyl sulfide - ≥99% , CAS No.538-74-9

CAS: 538-74-9 Cat. No.: D100593 Summenformel: C₁₄H₁₄S Molekulargewicht: 214.33 Beilstein Registry Number: 1911157 EG-Nummer: 208-703-6

GRADE & PURITY ≥99%

Synonyms

DTXSID6024599 | Benzene,1'-[thiobis(methylene)]bis- | DTXCID704599 | EINECS 208-703-6 | CAS-538-74-9 | Dibenzyl thioether | FT-0624646 | SULFIDE,DIBENZYL | Sulfide, dibenzyl | Sulfide, dibenzyl- | UNII-Q08048624M | B0440 | Dibenzyl sulphide | AI3-00842 |

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Übersicht

Sulfur K-edge XANES spectra of dibenzyl sulfide has been measured. Adsorption modes of dibenzyl disulphide on bare and iron-coated silver in 0.5M HCl was studied by surface-enhanced Raman scattering (SERS) spectroscopy. Dibenzyl sulfide undergoes oxidation to dibenzyl sulfoxide by SiO2-HNO3/KBr.

Specifications

Synonyme

DTXSID6024599 | Benzene,1'-[thiobis(methylene)]bis- | DTXCID704599 | EINECS 208-703-6 | CAS-538-74-9 | Dibenzyl thioether | FT-0624646 | SULFIDE,DIBENZYL | Sulfide, dibenzyl | Sulfide, dibenzyl- | UNII-Q08048624M | B0440 | Dibenzyl sulphide | AI3-00842 |

Spezifikationen & Reinheit

≥99%

Storage

Store at 2-8°C,Argon charged

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Reinheit

≥99%

Namen und Kennungen

• Pubchem Sid: 508812279
• Kanonisches Lächeln: C1=CC=C(C=C1)CSCC2=CC=CC=C2
• IUPAC Name: benzylsulfanylmethylbenzene
• InChIKey: LUFPJJNWMYZRQE-UHFFFAOYSA-N
• INCHI: 1S/C14H14S/c1-3-7-13(8-4-1)11-15-12-14-9-5-2-6-10-14/h1-10H,11-12H2
• Isomere SMILES: C1=CC=C(C=C1)CSCC2=CC=CC=C2
• WGK Deutschland: 2
• RTECS: DC0512500
• UN-Nummer: 3335
• Molekulargewicht: 214.33
• Beilstein: 1911157
• Reaxy-Rn: 1911157
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1911157&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Klasse Benzene and substituted derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Klasse: Benzene and substituted derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzene and substituted derivatives
• Alternative Parents: Sulfenyl compounds Dialkylthioethers Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Monocyclic benzene moiety - Dialkylthioether - Sulfenyl compound - Thioether - Hydrocarbon derivative - Organosulfur compound - Aromatic homomonocyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene.
• 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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PTH1R Tclin Parathyroid hormone receptor (47172 Activities)

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KCNH2 Tclin HERG (29587 Activities)

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GMNN Tbio Geminin (128009 Activities)

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CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)

Discover Target: CBX1

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

Discover Target: ATAD5

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ampC Beta-lactamase AmpC (62480 Activities)

Discover Target: ampC

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Wirkungsmechanismen

Chemische und physikalische Eigenschaften

• Empfindlichkeit: air sensitive
• Flammpunkt (°F): 230°F
• Flammpunkt (°C): 113 °C
• Siedepunkt (°C): 131 °C/2mmHg(lit.)
• Schmelzpunkt (°C): 49°C
• Molekulargewicht: 214.330 g/mol
• XLogP3: 3.900
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 4
• Exact Mass: 214.082 Da
• Monoisotopic Mass: 214.082 Da
• Topological Polar Surface Area: 25.300 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 137.000
• 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

Referenzen

1. Ziyi Wang, Ruimin Song, Weigen Chen, Jianxin Wang, Pinyi Wang, Zhixian Zhang, Xinyuan Zhang, Fu Wan.  (2022)  Vibrational Spectra and Molecular Vibrational Behaviors of Dibenzyl Disulfide, Dibenzyl Sulphide and Bibenzyl.  INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES,  23  (4): (1958).  [PMID:35216075] [10.3390/ijms23041958]

2. Ruotong Cui, Wenlong Xu, Yanpeng Zhang, Jingxian Wang, Yingyun Qiao, Yuanyu Tian.  (2025)  In-depth understanding of the rapid pyrolysis free radical reaction regulation mechanism of C-S bonds in coal at the molecular level.  FUEL,      [PMID:] [10.1016/j.fuel.2025.134630]

3. Xueao Jiang, Zhaoen Liu, Weijian Liu, Da Yu, Jun Zhang, Xiwen Wang, Yan Zhang, Shiguo Zhang.  (2024)  Physical ionogels with only 2 wt % gelators as efficient quasi-solid-state electrolytes for lithium batteries.  Matter,      [PMID:] [10.1016/j.matt.2024.01.021]

4. Huayu Liu, Lijia Liu, Yudan Wang, Fanshuai Gao, Yawen Liu.  (2025)  Preparation of disulfide bond-rich porous hypercrosslinked polymers for the efficient adsorption of trace methylmercury at ppb levels in aqueous solutions.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.163943]

5. Huayu Liu, Yahui Si, Lijia Liu, Yudan Wang, Fanshuai Gao, Yawen Liu.  (2025)  Preparation of hypercrosslinked porous polymer modified with paired thiol groups via in-situ disulfide bond cleavage for the rapid and efficient adsorption of mercury ions from water.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2025.133669]