Diclorodifenilsilanos - ≥97%(GC) , CAS No.80-10-4

CAS: 80-10-4 Cat. No.: D140820 Peso molecular: 253.2 Beilstein Registry Number: 609882 Número EC: 201-251-0

GRADE & PURITY ≥97%(GC)

Synonyms

Diclorodifenilsilano [checo] | Dicloro(difenil)silano | WLN: G-SI-GR&R | DICLORODIFENILSILANO | dicloro-difenil-silano | MFCD00000489 | NSC 77110 | D0362 | DTXSID2026494 | InChI=1/C12H10Cl2Si/c13-15(14,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10 | diclo

Storage

Argon charged,Room temperature

Shipped In

FedEx DG Service

Descripción general

Introducción del producto

El diclorodifenilsilano es un modificador de superficies a base de silano y un precursor que puede utilizarse en la síntesis de materiales a base de sílice. Se utiliza para modificar la superficie aportando dureza, durabilidad y resistencia a los golpes.

Aplicación

La reacción de adición de diclorodifenilsilano con diglicidil éter de bisfenol-S produce poli(silil éter) con grupos clorometilo colgantes. La reacción de acoplamiento entre el diclorometilsilano y el diclorodifenilsilano puede formar copolímeros de diorganosilano-hidrosilano a -75oC. El calentamiento del compuesto con tetrabutoxidianilinociclofosfazeno a temperaturas entre 100oC-160oC puede producir oligómeros de ciclofosfazeno.

Specifications

Sinónimos

Diclorodifenilsilano [checo] | Dicloro(difenil)silano | WLN: G-SI-GR&R | DICLORODIFENILSILANO | dicloro-difenil-silano | MFCD00000489 | NSC 77110 | D0362 | DTXSID2026494 | InChI=1/C12H10Cl2Si/c13-15(14, 11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10 | diclo

Especificaciones y pureza

≥97%(GC)

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

FedEx DG Service

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥97%(GC)

Nombres e identificadores

• Pubchem Sid: 504751141
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504751141
• Sonrisas canónicas: C1=CC=C(C=C1)[Si](C2=CC=CC=C2)(Cl)Cl
• IUPAC Name: dichloro(diphenyl)silane
• InChIKey: OSXYHAQZDCICNX-UHFFFAOYSA-N
• INCHI: 1S/C12H10Cl2Si/c13-15(14,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H
• Isómeros SMILES: C1=CC=C(C=C1)[Si](C2=CC=CC=C2)(Cl)Cl
• WGK Alemania: 1
• RTECS: VV3190000
• Número ONU: 1769
• Grupo de embalaje: II
• Peso molecular: 253.2
• Beilstein: 609882
• Reaxy-Rn: 609882
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=609882&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzene and substituted derivatives
• Alternative Parents: Organochlorosilanes Organic metalloid salts Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Monocyclic benzene moiety - Organoheterosilane - Organochlorosilane - Organic metalloid salt - Hydrocarbon derivative - Organic salt - Organosilicon compound - Aromatic homomonocyclic compound
• Descripción: 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

Objetivos asociados (no humanos)

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Solubility in water: Decomposes
• Sensibilidad: Moisture Sensitive.
• Índice de refracción: 1.581
• Punto de inflamación (°F): 287.6 °F
• Punto de inflamación (°C): 142 °C
• Punto de ebullición (°C): 305 °C
• Punto de fusión (°C): -22℃
• Peso molecular: 253.190 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 2
• Exact Mass: 251.993 Da
• Monoisotopic Mass: 251.993 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 15
• Formal Charge: 0
• Complexity: 174.000
• 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

XLogP3

Referencias

1. Xiaohan Li, Qiunan Xie, Jieying Lin, Jiateng Huang, Kaili Xie, Jingcheng Liu, Xiaojie Li, Wei Wei.  (2023)  A phosphorus/silicon-containing flame retardant based on eugenol for improving flame retardancy and smoke suppression of epoxy resin.  JOURNAL OF APPLIED POLYMER SCIENCE,  140  (39): (e54474).  [PMID:] [10.1002/app.54474]

2. Siyuan He, Cheng Chi, Chaohua Peng, Birong Zeng, Yongming Chen, Zhongxi Miao, Hui Xu, Weiang Luo, Guorong Chen, Zhenping Fu, Lizong Dai.  (2023)  A Novel P/N/Si-Containing Vanillin-Based Compound for a Flame-Retardant, Tough Yet Strong Epoxy Thermoset.  Polymers,  15  (10): (2384).  [PMID:37242961] [10.3390/polym15102384]

3. Ji-Hao Zuo, Yi-Hang Gu, Chao Wei, Xi Yan, Yan Chen, Wan-Zhong Lang.  (2019)  Janus polyvinylidene fluoride membranes fabricated with thermally induced phase separation and spray-coating technique for the separations of both W/O and O/W emulsions.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2019.117475]

4. Peng Yang, Mengyuan Ren, Kongfa Chen, Yu Liang, Qiu-Feng Lü, Teng Zhang.  (2019)  Synthesis of a novel silicon-containing epoxy resin and its effect on flame retardancy, thermal, and mechanical properties of thermosetting resins.  Materials Today Communications,      [PMID:] [10.1016/j.mtcomm.2019.01.014]

5. Manman Jin, Jinkai Wang, Bing Wang, Zhenmei Guo, Zhiguo Lv.  (2018)  Highly effective green oxidation of aldehydes catalysed by recyclable tungsten complex immobilized in organosilanes-modified SBA-15.  MICROPOROUS AND MESOPOROUS MATERIALS,      [PMID:] [10.1016/j.micromeso.2018.10.021]

6. Yong Tang, Xiyu Zhang, Zheng Liu, Xiaoya Liu, Xiaojie Li.  (2025)  A resveratrol-based P/Si-containing hyperbranched flame retardant for simultaneously enhancing fire safety and mechanical properties of epoxy thermosets.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.160240]

7. Xueying Shan, Qixin Huang, Yuxuan Diao, Boyou Hou, Jiao Gao, Jinchun Li.  (2025)  A Schiff base-derived macromolecular flame retardant: Imparting excellent flame retardancy, UV shielding, and mechanical properties to epoxy resins.  PROGRESS IN ORGANIC COATINGS,      [PMID:] [10.1016/j.porgcoat.2025.109437]

8. Junbo Zang, Jiahui Qi, Jiaxu Zhang, Hao Liu, Chunhong Zhang, Chengyue Zhang, Runtian Wu, Xiaochao Xu, Lei Shang.  (2026)  High-strength, flame-retardant, dielectric Si-functionalized biomass hybrid crosslinked non-isocyanate polyurethane-epoxy for general-purpose adhesive.  POLYMER DEGRADATION AND STABILITY,      [PMID:] [10.1016/j.polymdegradstab.2026.111997]

9. Zhenyang Yin, Yitong Jiang, Fengyu Meng, Xiaoming Qi, Jiangsheng Chen, Hongbo Dai, Chen Qian, Yaqin Fu.  (2026)  Nacre-Inspired Flame-Retardant Coating with a Brick–Mortar Architecture Based on Bio-Based Chitosan/Gelatin and APP/MMT for Flexible Polyurethane Foam.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.5c04018]