Chlorotriethoxysilane - ≥95%(GC) , CAS No.4667-99-6

CAS: 4667-99-6 Cat. No.: C153551 분자식: C₆H₁₅ClO₃Si 분자량: 198.72 EC 번호: 225-112-9

GRADE & PURITY ≥95%(GC)

Synonyms

Chlorotriethoxysilane, 98% | Chloro(triethoxy)silane | MFCD00015124 | C3354 | triethoxysilyl chloride | SCHEMBL155200 | Silane, chlorotriethoxy- | AKOS015915892 | Triethoxychlorosilane | triethoxy-chloro-silane | Chloro(triethoxy)silane # | ClSi(OEt)3 | C

Storage

Store at 2-8°C,Argon charged,Desiccated

Shipped In

Wet ice

Specifications

동의어

Chlorotriethoxysilane, 98% | Chloro(triethoxy)silane | MFCD00015124 | C3354 | triethoxysilyl chloride | SCHEMBL155200 | Silane, chlorotriethoxy- | AKOS015915892 | Triethoxychlorosilane | triethoxy-chloro-silane | Chloro(triethoxy)silane # | ClSi(OEt)3 | C

사양 및 순도

≥95%(GC)

보관 조건

Store at 2-8°C,Argon charged,Desiccated

배송

Wet ice

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순수함

≥95%(GC)

이름과 식별자

• Pubchem Sid: 508814179
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/508814179
• 정식 스마일: CCO[Si](OCC)(OCC)Cl
• IUPAC Name: chloro(triethoxy)silane
• InChIKey: JEZFASCUIZYYEV-UHFFFAOYSA-N
• INCHI: 1S/C6H15ClO3Si/c1-4-8-11(7,9-5-2)10-6-3/h4-6H2,1-3H3
• 이성체 SMILES: CCO[Si](OCC)(OCC)Cl
• WGK 독일: 3
• 분자량: 198.72
• Reaxy-Rn: 1745173
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1745173&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • 분류 Organometalloid compounds
      • Subclass Organosilicon compounds

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• 분류: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Not available
• Direct Parent: Alkoxysilanes
• Alternative Parents: Organic metalloid salts Organooxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alkoxysilane - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Aliphatic acyclic compound
• 설명: This compound belongs to the class of organic compounds known as alkoxysilanes. These are organosilicon compounds with the general formula RO[Si](OR')(R'')(R''') (R,R' = organyl; R'',R''' = any atom).
• 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

화학 및 물리적 특성

• 감도: Moisture Sensitive,Heat Sensitive
• 굴절률: 1.39
• 발화점(°F): 116.6 °F
• 발화점(°C): 47°C
• 끓는점(°C): 156-157 °C
• 분자량: 198.720 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 6
• Exact Mass: 198.048 Da
• Monoisotopic Mass: 198.048 Da
• Topological Polar Surface Area: 27.700 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 84.800
• 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

XLogP3

참고 문헌

1. Xiaoyun Qiao, Zeshan Xiong, Zongtao Zhang, Runwei Wang, Shilun Qiu.  (2022)  Periodic mesoporous organosilica functionalized hollow TiO2 sphere for selective aerobic oxidation.  APPLIED SURFACE SCIENCE,      [PMID:] [10.1016/j.apsusc.2022.155182]

2. Huamei Zhu, Chaoen Jin, Fan Wang, Yaping Zhu, Shifeng Deng, Huimin Qi.  (2025)  Synthesis and characterization of silicon-containing arylacetylene resins-like heat-resistant silane coupling agents: Enhancement of interfacial properties for composites.  POLYMER COMPOSITES,      [PMID:] [10.1002/pc.29601]

3. Xin Wang, Lihong He, Jianrong Huang, Nanjing Zhong.  (2020)  Immobilization of lipases onto the halogen & haloalkanes modified SBA-15: Enzymatic activity and glycerolysis performance study.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:33345972] [10.1016/j.ijbiomac.2020.12.111]