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78704-49-1

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78704-49-1 Usage

General Description

(4-Chlorophenylethynyl)trimethylsilane is an organosilicon compound that has a molecular formula of C10H11ClSi. It is commonly used as a building block in organic synthesis and is often utilized in the production of pharmaceuticals and agrochemicals. (4-CHLOROPHENYLETHYNYL)TRIMETHYLSILANE is a clear, colorless liquid with a strong odor and is highly flammable. It is also known to be a skin and eye irritant and should be handled with care. The (4-chlorophenylethynyl) group is a reactive component that can undergo various synthetic transformations, making this compound valuable in the field of organic chemistry. Additionally, the trimethylsilyl group provides stability and protection for other functional groups in the molecule. Overall, (4-Chlorophenylethynyl)trimethylsilane is an important reagent in organic synthesis with a wide range of applications in the pharmaceutical and agrochemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 78704-49-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,7,0 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78704-49:
(7*7)+(6*8)+(5*7)+(4*0)+(3*4)+(2*4)+(1*9)=161
161 % 10 = 1
So 78704-49-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H13ClSi/c1-13(2,3)9-8-10-4-6-11(12)7-5-10/h4-7H,1-3H3

78704-49-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H55129)  (4-Chlorophenylethynyl)trimethylsilane, 97%   

  • 78704-49-1

  • 1g

  • 165.0CNY

  • Detail
  • Alfa Aesar

  • (H55129)  (4-Chlorophenylethynyl)trimethylsilane, 97%   

  • 78704-49-1

  • 5g

  • 972.0CNY

  • Detail
  • Alfa Aesar

  • (H55129)  (4-Chlorophenylethynyl)trimethylsilane, 97%   

  • 78704-49-1

  • 25g

  • 4858.0CNY

  • Detail
  • Aldrich

  • (563447)  (4-Chlorophenylethynyl)trimethylsilane  97%

  • 78704-49-1

  • 563447-5G

  • 783.90CNY

  • Detail

78704-49-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorophenyl)ethynyl-trimethylsilane

1.2 Other means of identification

Product number -
Other names (2-(4-chlorophenyl)ethynyl)trimethylsilane

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:78704-49-1 SDS

78704-49-1Relevant articles and documents

Iodonium Cation-Pool Electrolysis for the Three-Component Synthesis of 1,3-Oxazoles

Sattler, Lars E.,Hilt, Gerhard

supporting information, p. 605 - 608 (2020/12/07)

The synthesis of 1,3-oxazoles from symmetrical and unsymmetrical alkynes was realized by an iodonium cation-pool electrolysis of I2 in acetonitrile with a well-defined water content. Mechanistic investigations suggest that the alkyne reacts with the acetonitrile-stabilized I+ ions, followed by a Ritter-type reaction of the solvent to a nitrilium ion, which is then attacked by water. The ring closure to the 1,3-oxazoles released molecular iodine, which was visible by the naked eye. Also, some unsymmetrical internal alkynes were tested and a regioselective formation of a single isomer was determined by two-dimensional NMR experiments.

Cobalt-Catalyzed Hydroalkynylation of Vinylaziridines

Biletskyi, Bohdan,Kong, Lingyu,Tenaglia, Alphonse,Clavier, Hervé

supporting information, p. 2578 - 2585 (2021/03/18)

Transition metal-catalyzed hydroalkynylation reactions are efficient transformations allowing the straightforward formation of functionalized alkynes. Therein, we disclose the cobalt-catalyzed hydroalkynylation of vinylaziridines giving rise to both linea

Synthesis and Photochemical Application of Hydrofluoroolefin (HFO) Based Fluoroalkyl Building Block

Varga, Bálint,Tóth, Balázs L.,Béke, Ferenc,Csenki, János T.,Kotschy, András,Novák, Zoltán

supporting information, p. 4925 - 4929 (2021/07/01)

A novel fluoroalkyl iodide was synthesized on multigram scale from refrigerant gas HFO-1234yf as cheap industrial starting material in a simple, solvent-free, and easily scalable process. We demonstrated its applicability in a metal-free photocatalytic ATRA reaction to synthesize valuable fluoroalkylated vinyl iodides and proved the straightforward transformability of the products in cross-coupling chemistry to obtain conjugated systems.

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