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224,000+ research products · Triple ISO certified · COA & SDS available for every product · Same-day shipping on in-stock items 1,2-Bis(trimethylsilyl)benzene - ≥95% , CAS No.17151-09-6
Synonyms
T70415 | Silane, 1,2-phenylenebis[trimethyl- | B2299 | 2-(((4-bromophenyl)sulfonyl)amino)-benzoicaci | Trimethyl[2-(trimethylsilyl)phenyl]silane | AKOS015840092 | FT-0723705 | DTXSID30334143 | trimethyl-(2-trimethylsilylphenyl)silane | SY053637 | Trimethy
Storage
Store at 2-8°C,Argon charged
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Why this grade ≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
T70415 | Silane, 1, 2-phenylenebis[trimethyl- | B2299 | 2-(((4-bromophenyl)sulfonyl)amino)-benzoicaci | Trimethyl[2-(trimethylsilyl)phenyl]silane | AKOS015840092 | FT-0723705 | DTXSID30334143 | trimethyl-(2-trimethylsilylphenyl)silane | SY053637 | Trimethy
Specifications & Purity
≥95%
Storage
Store at 2-8°C, Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Names and Identifiers Canonical Smiles C[Si](C)(C)C1=CC=CC=C1[Si](C)(C)C IUPAC Name trimethyl-(2-trimethylsilylphenyl)silane InChIKey YHMJZIJXVNRXIN-UHFFFAOYSA-N INCHI 1S/C12H22Si2/c1-13(2,3)11-9-7-8-10-12(11)14(4,5)6/h7-10H,1-6H3 Isomeric SMILES C[Si](C)(C)C1=CC=CC=C1[Si](C)(C)C Molecular Weight 222.48 Reaxy-Rn 2937659 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2937659&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organometallic compounds Class Organometalloid compounds Subclass Organosilicon compounds Intermediate Tree Nodes Not available Direct Parent Alkylarylsilanes Alternative Parents Benzene and substituted derivatives Organic metalloid salts Hydrocarbon derivatives Alkylsilanes Molecular Framework Aromatic homomonocyclic compounds Substituents Alkylarylsilane - Benzenoid - Monocyclic benzene moiety - Organic metalloid salt - Hydrocarbon derivative - Organic salt - Alkylsilane - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as alkylarylsilanes. These are organosilicon compounds with the general formula R[Si]R' (R = alkyl, R' = aryl). 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.
3D Structure Certificates(CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Sensitivity Air Sensitive,Heat Sensitive Refractive Index 1.51 Flash Point(°C) 90 °C Molecular Weight 222.470 g/mol XLogP3 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 0 Rotatable Bond Count 2 Exact Mass 222.126 Da Monoisotopic Mass 222.126 Da Topological Polar Surface Area 0.000 Ų Heavy Atom Count 14 Formal Charge 0 Complexity 163.000 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
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