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BIS(PHENYLETHYNYL)DIMETHYLSILANE, an organic compound containing silicon, is characterized by its molecular formula C20H16Si. This indicates that it is composed of 20 carbon atoms, 16 hydrogen atoms, and 1 silicon atom. It is a clear to pale yellow substance, known for its high-temperature resistance, which makes it suitable for the production of heat-resistant polymers. With a molar mass of 284.41 grams per mole and a boiling point around 420 degrees Celsius, BIS(PHENYLETHYNYL)DIMETHYLSILANE can be synthesized through the reaction of dimethyldichlorosilane with phenylacetylene.

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  • 2170-08-3 Structure
  • Basic information

    1. Product Name: BIS(PHENYLETHYNYL)DIMETHYLSILANE
    2. Synonyms: Dimethylbis(phenylethynyl)silane
    3. CAS NO:2170-08-3
    4. Molecular Formula: C18H16Si
    5. Molecular Weight: 260.41
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2170-08-3.mol
  • Chemical Properties

    1. Melting Point: 78-81°C
    2. Boiling Point: 180°C 4mm
    3. Flash Point: >110°C
    4. Appearance: /
    5. Density: 1.03g/cm3
    6. Vapor Pressure: 5.32E-05mmHg at 25°C
    7. Refractive Index: 1.584
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: BIS(PHENYLETHYNYL)DIMETHYLSILANE(CAS DataBase Reference)
    11. NIST Chemistry Reference: BIS(PHENYLETHYNYL)DIMETHYLSILANE(2170-08-3)
    12. EPA Substance Registry System: BIS(PHENYLETHYNYL)DIMETHYLSILANE(2170-08-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: 36/37/38
    3. Safety Statements: 26-36/37/39
    4. WGK Germany:
    5. RTECS:
    6. TSCA: No
    7. HazardClass: N/A
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 2170-08-3(Hazardous Substances Data)

2170-08-3 Usage

Uses

Used in High-Temperature Polymers Industry:
BIS(PHENYLETHYNYL)DIMETHYLSILANE is used as a key component for the production of high-temperature polymers due to its heat resistance properties. This allows the creation of materials that can withstand extreme thermal conditions, which is crucial in various industrial applications.
Used in Chemical Synthesis:
BIS(PHENYLETHYNYL)DIMETHYLSILANE is used as a starting material or intermediate in the synthesis of other complex organic compounds, particularly those that require silicon-containing structures. Its versatility in chemical reactions makes it a valuable asset in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 2170-08-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,7 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2170-08:
(6*2)+(5*1)+(4*7)+(3*0)+(2*0)+(1*8)=53
53 % 10 = 3
So 2170-08-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H16Si/c1-19(2,15-13-17-9-5-3-6-10-17)16-14-18-11-7-4-8-12-18/h3-12H,1-2H3

2170-08-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl-bis(2-phenylethynyl)silane

1.2 Other means of identification

Product number -
Other names LRBLIVYQOCFXPX-UHFFFAOYSA

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2170-08-3 SDS

2170-08-3Relevant articles and documents

Experimental and theoretical studies of magnetic exchange in silole-bridged diradicals

Roques, Nans,Gerbier, Philippe,Schatzschneider, Ulrich,Sutter, Jean-Pascal,Guionneau, Philippe,Vidal-Gancedo, Jose,Veciana, Jaume,Rentschler, Eva,Guerin, Christian

, p. 5547 - 5562 (2006)

Five bis(tert-butylnitroxide) diradicals connected by a silole (7a-d) or a thiophene (12) ring as a coupler were studied. Compound 12 crystallizes in the orthorhombic space group Pna21 with a = 20.752(5), b = 5.826(5), and c = 34.309(5) A. X-ra

Electrochemiluminescence Platforms Based on Small Water-Insoluble Organic Molecules for Ultrasensitive Aqueous-Phase Detection

Han, Zhengang,Yang, Zhaofan,Sun, Heshui,Xu, Yali,Ma, Xiaofang,Shan, Duoliang,Chen, Jing,Huo, Shuhui,Zhang, Zhen,Du, Peiyao,Lu, Xiaoquan

, p. 5915 - 5919 (2019)

Highly efficient detection in the aqueous phase for water-insoluble organic molecule probes is challenging. The bright aggregated-state electrochemiluminescence (ECL) of 1,1-disubstituted 2,3,4,5-tetraphenylsiloles by a co-reactant approach was discovered

Catalytic Decarboxylation of Silyl Alkynoates to Alkynylsilanes

Aoyagi, Keiya,Choi, Jun-Chul,Kawatsu, Takahiro,Matsumoto, Kazuhiro,Nakajima, Yumiko,Sato, Kazuhiko

supporting information, (2020/09/15)

Herein, we describe a decarboxylative approach to the preparation of alkynylsilanes. Treatment of a silyl alkynoate in N,N-dimethylformamide (DMF) at 80 °C in the presence of catalytic amounts of CuCl and PCy3 produced the corresponding alkynylsilane in excellent yield. The copper-catalyzed decarboxylation proceeded smoothly with low catalyst loadings (0.5 mol % of CuCl and 1.0 mol % of PCy3) under mild reaction conditions and is easily scalable to gram quantities.

METHOD FOR PRODUCING ORGANOSILICON COMPOUND USING HALOSILANE AS RAW MATERIAL

-

Paragraph 0044-0045; 0055, (2019/12/10)

PROBLEM TO BE SOLVED: To provide a novel method for producing an organosilicon compound. SOLUTION: The method for producing an organosilicon compound includes a reaction step (I) of reacting a halosilane represented by formula (a) with a compound containing a hydrocarbon group represented by formula (b) in the presence of an organic base to generate an organosilicon compound represented by formula (c). (In the formula (I), n is an integer of 0-3; each R1 independently represents a hydrogen atom or a C1-20 hydrocarbon group which may contain a heteroatom; X represents a bromo group (-Br) or a chloro group (-Cl); and R2 represents a compound containing a hydrocarbon group.) SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2020,JPOandINPIT

Water-soluble AIE luminogens for monitoring and retardation of fibrillation of amyloid proteins

-

Page/Page column 67, (2016/04/20)

Compounds that exhibit aggregation induced emission (AIE), and more particularly to water-soluble conjugated polyene compounds that exhibit aggregation induced emission. The conjugated polyene compounds can be used as bioprobes for DNA detection, G-quadru

Siloles and acetenyl aromatics copolymers: Synthesis, characterization and photophysical properties

He, Zhenhua,Lai, Guoqiao,Li, Zhifang,Yuan, Xiao,Shen, Yongjia,Wang, Chengyun

, p. 550 - 558 (2015/05/27)

Two copolymers, poly(1,1-dimethyl-3,4-diphenylsilole-alt-N-hexyl-3,6-diethynylcarbazole) (PS-DyCz) and poly(1,1-dimethyl-3,4-diphenylsilole-alt-2,7-diethynyl-9,9′-dihexylfluorene) (PS-DyF), were synthesized by Sonogashira coupling reaction of 2,5-dibromo-

Iridium-promoted conversion of chlorosilanes to alkynyl derivatives in a one-pot reaction sequence

Kownacki, Ireneusz,Orwat, Bartosz,Marciniec, Bogdan

supporting information, p. 3051 - 3059 (2014/07/08)

By making use of the catalytic potential of the iridium system [{Ir(μ-Cl)(CO)2}2]/NEt(i-Pr)2 in the synthesis of silyl-functionalized alkynes via silylative coupling of terminal alkynes/diynes with iodosilanes, we propose

Grignard metathesis polymerization and properties of 1,1-disubstituted-2,5- dibromo-3,4-diphenylsiloles

Park, Young Tae

, p. 1825 - 1831 (2014/07/07)

Grignard metathesis polymerizations of 1,1-disubstituted-2,5-dibromo-3,4- diphenylsiloles such as 1,1-dimethyl-2,5-dibromo-3,4-diphenylsilole, 1,1-diethyl-2,5-dibromo-3,4-diphenylsilole, 1,1-diisopropyl-2,5-dibromo-3,4- diphenylsilole, and 1,1-dihexyl-2,5

Biocompatible Nanoparticles with Aggregation Induced Emission Characteristics as Fluorescent Bioprobes and Methods of Using the Same for In Vitro and In Vivo Imaging

-

Page/Page column, (2014/11/13)

The development of fluorescent bioprobes comprising organic fluorescent compounds that exhibit aggregation induced emission (AIE) properties, methods of producing the same, and their practical applications for in vitro and in vivo bioimaging.

Conjugation versus rotation: Good conjugation weakens the aggregation-induced emission effect of siloles

Chen, Bin,Nie, Han,Lu, Ping,Zhou, Jian,Qin, Anjun,Qiu, Huayu,Zhao, Zujin,Tang, Ben Zhong

supporting information, p. 4500 - 4503 (2014/04/17)

Incorporation of polycyclic aromatic hydrocarbons into siloles enhances their light emission in solutions but lowers emission efficiency in the aggregated state. The competitive interaction between conjugation and rotation is thus studied. This journal is

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