1,4-Bis(triethoxysilyl)benzene（BTEB） - ≥96% , CAS No.2615-18-1

CAS: 2615-18-1 Cat. No.: B169119 Peso molecular: 402.63 Número EC: 860-806-0

GRADE & PURITY ≥96%

Synonyms

CAA61518 | DTXSID10467564 | A848366 | J-016284 | YYJNCOSWWOMZHX-UHFFFAOYSA-N | 14-Bis(Triethoxysilyl)Benzene | SCHEMBL50701 | 1,4-BIS(TRIETHOXYSILYL)BENZENE 96 | TRIETHOXY[4-(TRIETHOXYSILYL)PHENYL]SILANE | AKOS015889133 | Triethoxy-(4-triethoxysilylphenyl

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

1,4-Bis(triethoxysilyl)benzene (BTEB) is a silicon-based nucleophile shown to be reactive in Pd-catalyzed cross-coupling reactions. It is extensively used as a precursor in the synthesis of a variety of periodic mesoporous organosilicas (PMOs).

Specifications

Sinónimos

CAA61518 | DTXSID10467564 | A848366 | J-016284 | YYJNCOSWWOMZHX-UHFFFAOYSA-N | 14-Bis(Triethoxysilyl)Benzene | SCHEMBL50701 | 1, 4-BIS(TRIETHOXYSILYL)BENZENE 96 | TRIETHOXY[4-(TRIETHOXYSILYL)PHENYL]SILANE | AKOS015889133 | Triethoxy-(4-triethoxysilylphenyl

Especificaciones y pureza

≥96%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥96%

Nombres e identificadores

• Pubchem Sid: 504766485
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504766485
• Sonrisas canónicas: CCO[Si](C1=CC=C(C=C1)[Si](OCC)(OCC)OCC)(OCC)OCC
• IUPAC Name: triethoxy-(4-triethoxysilylphenyl)silane
• InChIKey: YYJNCOSWWOMZHX-UHFFFAOYSA-N
• INCHI: 1S/C18H34O6Si2/c1-7-19-25(20-8-2,21-9-3)17-13-15-18(16-14-17)26(22-10-4,23-11-5)24-12-6/h13-16H,7-12H2,1-6H3
• Isómeros SMILES: CCO[Si](C1=CC=C(C=C1)[Si](OCC)(OCC)OCC)(OCC)OCC
• WGK Alemania: 3
• Peso molecular: 402.63
• Reaxy-Rn: 3009005
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3009005&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Clase Organometalloid compounds
      • Subclass Organosilicon compounds
        • Level5 Alkoxysilanes
          • Level6 Trialkoxysilanes

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Clase: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Alkoxysilanes
• Direct Parent: Trialkoxysilanes
• Alternative Parents: Benzene and substituted derivatives Silyl ethers Organoheterosilanes Organic metalloid salts Organooxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Trialkoxysilane - Benzenoid - Monocyclic benzene moiety - Silyl ether - Organoheterosilane - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Aromatic homomonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as trialkoxysilanes. These are organosilicon compounds with the general formula RO[Si](R')(OR'')OR''' (R-R''' = aliphatic organyl group).
• 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

Propiedades químicas y físicas

• Sensibilidad: Hygroscopic
• Índice de refracción: n20/D 1.456
• Punto de inflamación (°F): >230 °F
• Punto de inflamación (°C): >110 °C
• Punto de ebullición (°C): 130-133 °C/0.5 mmHg
• Peso molecular: 402.600 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 14
• Exact Mass: 402.189 Da
• Monoisotopic Mass: 402.189 Da
• Topological Polar Surface Area: 55.400 Ų
• Heavy Atom Count: 26
• Formal Charge: 0
• Complexity: 296.000
• 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. Shichun Gu, Ruyi Wang, Junxiong Zhang, Hairong Dong, Liping Deng, Xue Wang, Yapeng He.  (2023)  One-step synthesis of hollow and yolk-shell mesoporous organosilica nanospheres for efficient separation of lead ions.  MICROPOROUS AND MESOPOROUS MATERIALS,      [PMID:] [10.1016/j.micromeso.2023.112884]

2. Yang Ling, Yan Peng, Shiyou Guan.  (2023)  Facile Synthesis of SiOx/C Composite with Homogeneous Distribution of SiOx and Carbon as Anodes for Superior Lithium-Ion Batteries.  ChemistrySelect,  8  (16): (e202300233).  [PMID:] [10.1002/slct.202300233]

3. Meng Cheng, Junhao Liu, Yuqi Liu, Hao Jiang, Chunling Li, Shuangqing Sun, Songqing Hu.  (2023)  Three birds with one stone: Contemporaneously boosting passive, active and self-healing properties for long-term anticorrosion coatings.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.141532]

4. Yang Ling, Yuan Gao, Yan Peng, Shiyou Guan.  (2022)  Carbon Uniformly Distributed SiOx/C Composite with Excellent Structure Stability for High Performance Lithium-Ion Batteries.  Chemistry-An Asian Journal,  17  (11): (e202200202).  [PMID:35475574] [10.1002/asia.202200202]

5. Huang Yi, Zhao Chenyang, Li Yue, Wang Chen, Yuan Wenlin, Cheng Di, Shen Tao, Zhang Ji, Liu Jie, Shen Qianhong, Yang Hui.  (2025)  Sol-gel coating prepared using pH-responsive hollow porous organosilica nanocontainers encapsulating 2-mercaptobenzothiazole for enhanced corrosion resistance of aluminum alloy.  JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY,      [PMID:] [10.1007/s10971-025-06677-w]

6. Bokai Zhou, Jie Feng, Yi Zhang, Ting Zhang, Caiwei Hu, Shuyan Liu, Xu Yin, Mingshi Jin, Yu Bai.  (2025)  Bifunctional bowl-shaped organosilica for efficient exosome capture and metabolites panel based hepatocellular carcinoma diagnosis.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.163980]

7. Xuemeng Xu, Xiaxing Feng, Shuang Wang, Yuhong Lin, Bing Wang, Yaming Sun, Chenchen Song, Lijun He, Ke Zhang.  (2025)  Controllable multipods periodic mesoporous organosilica modified with ionic liquid and application in simultaneous and accurate detection of aflatoxin B1 and its biosynthetic precursors in cereals.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:41191995] [10.1016/j.chroma.2025.466500]