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Silane, (4-ethynylphenyl)trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 16116-92-0 Structure
  • Basic information

    1. Product Name: Silane, (4-ethynylphenyl)trimethyl-
    2. Synonyms:
    3. CAS NO:16116-92-0
    4. Molecular Formula: C11H14Si
    5. Molecular Weight: 174.318
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 16116-92-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Silane, (4-ethynylphenyl)trimethyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Silane, (4-ethynylphenyl)trimethyl-(16116-92-0)
    11. EPA Substance Registry System: Silane, (4-ethynylphenyl)trimethyl-(16116-92-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 16116-92-0(Hazardous Substances Data)

16116-92-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16116-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,1,1 and 6 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 16116-92:
(7*1)+(6*6)+(5*1)+(4*1)+(3*6)+(2*9)+(1*2)=90
90 % 10 = 0
So 16116-92-0 is a valid CAS Registry Number.

16116-92-0Relevant articles and documents

PEST CONTROL AGENT

-

Paragraph 0112, (2016/10/09)

PROBLEM TO BE SOLVED: To provide a compound having high activity to pest, a pest control agent obtained using the compound and a method for controlling pest by application of the compound. SOLUTION: The present invention provides the pest control agent co

Click polymerization: Synthesis of novel σ-π Conjugated organosilicon polymers

Wang, Yike,Wang, Dengxu,Xu, Caihong,Wang, Rui,Han, Jianjun,Feng, Shengyu

experimental part, p. 3000 - 3005 (2011/09/15)

Poly[silylene-1,4-phenylene-(1,2,3-triazol-4-yl)-1,4-phenylene]s were prepared via step-growth Click coupling polymerization of bis(p-ethynylphenyl) silanes and 1,4-diazidobenzene. The organosilicon units in the backbones may contribute to an electronic c

Synthesis and electro-optical properties of 9,10-substituted anthracene derivatives for flexible OLED devices

Han, Yoon Soo,Jeong, Seonju,Ryu, Sang Chul,Park, Eun Jung,Lyu, Eon Joo,Kwak, Giseop,Park, Lee Soon

experimental part, p. 163 - 178 (2010/07/15)

A silylated anthracene derivative, bis[2-(p-trimethylsilyl)phenylethynyl] anthracene (1), was synthesized by using Sonogashira reaction. Compound 1 showed two absorption maxia(max,abs) at 444 and 447nm, and fluorescence maximum (max,em) at 478nm. Compound

Compounds 620

-

Page/Page column 13, (2008/12/06)

This invention relates to novel compounds having the structural formula I below: and to their pharmaceutically acceptable salt, compositions and methods of use. These novel compounds provide a treatment or prophylaxis of cognitive impairment, Alzheimer Disease, neurodegeneration and dementia.

Synthesis and properties of F-containing poly(diphenylacetylene) membranes

Sakaguchi, Toshikazu,Shiotsuki, Masashi,Sanda, Fumio,Freeman, Benny D.,Masuda, Toshio

, p. 8327 - 8332 (2008/02/02)

The polymerization of various silyl- and F-containing diphenylacetylenes (1a-k) with TaCl5-n-Bu4Sn provided high-molecular-weight polymers. Most polymers (2a-d, 2g, and 2h) were totally soluble in common organic solvents and afforded

Oligomers of hexa-peri-hexabenzocoronenes as "super- oligophenylenes": Synthesis, electronic properties, and self-assembly

Wu, Jishan,Watson, Mark D.,Tchebotareva, Natalia,Wang, Zhaohui,Muellen, Klaus

, p. 8194 - 8204 (2007/10/03)

Hexa-peri-hexabenzocoronene (HBC) is a remarkable polycyclic aromatic hydrocarbon and is often called "superbenzene" because of its similarity to benzene. In this article we present the facile synthesis of oligomers of HBC, up to trimers (3, 4, 5a-c) with

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