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2-(3-METHOXY-1-PROPYN-1-YL)-4,4,5,5-TETRAMETHYL-(1,3,2)DIOXABOROLANE is an alkynylboronate compound that plays a significant role in various chemical reactions and processes due to its unique structure and properties.

634196-63-7

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634196-63-7 Usage

Uses

Used in Chemical Synthesis:
2-(3-METHOXY-1-PROPYN-1-YL)-4,4,5,5-TETRAMETHYL-(1,3,2)DIOXABOROLANE is used as a key intermediate in the synthesis of complex organic molecules for various applications, including pharmaceuticals and materials science. Its unique structure allows for regioand stereoselective carbon-carbon bond formation, which is crucial for the development of novel compounds with specific properties.
Used in Enyne Cross-Metathesis:
In the field of organic chemistry, 2-(3-METHOXY-1-PROPYN-1-YL)-4,4,5,5-TETRAMETHYL-(1,3,2)DIOXABOROLANE is used as a reactant in enyne cross-metathesis reactions. This reaction is an important tool for the formation of new carbon-carbon bonds, which are essential for the synthesis of complex organic molecules.
Used in Alder Ene Reaction:
2-(3-METHOXY-1-PROPYN-1-YL)-4,4,5,5-TETRAMETHYL-(1,3,2)DIOXABOROLANE also participates in the Alder ene reaction, which is a powerful method for the formation of carbon-carbon bonds with high stereoselectivity. This reaction is particularly useful in the synthesis of natural products and complex molecular structures.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(3-METHOXY-1-PROPYN-1-YL)-4,4,5,5-TETRAMETHYL-(1,3,2)DIOXABOROLANE is used as a building block for the development of new drugs. Its unique reactivity and selectivity in various chemical reactions enable the creation of novel drug candidates with improved efficacy and selectivity.
Used in Materials Science:
In materials science, 2-(3-METHOXY-1-PROPYN-1-YL)-4,4,5,5-TETRAMETHYL-(1,3,2)DIOXABOROLANE is used in the synthesis of advanced materials with specific properties, such as improved mechanical strength, thermal stability, or electrical conductivity. These materials can be used in various applications, including aerospace, electronics, and energy storage.

Check Digit Verification of cas no

The CAS Registry Mumber 634196-63-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,4,1,9 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 634196-63:
(8*6)+(7*3)+(6*4)+(5*1)+(4*9)+(3*6)+(2*6)+(1*3)=167
167 % 10 = 7
So 634196-63-7 is a valid CAS Registry Number.

634196-63-7 Well-known Company Product Price

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  • Aldrich

  • (674710)  3-Methoxy-1-propyn-1-ylboronicacidpinacolester  96%

  • 634196-63-7

  • 674710-1G

  • 1,044.81CNY

  • Detail
  • Aldrich

  • (674710)  3-Methoxy-1-propyn-1-ylboronicacidpinacolester  96%

  • 634196-63-7

  • 674710-5G

  • 3,696.03CNY

  • Detail

634196-63-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-methoxyprop-1-ynyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names 2-(3-Methoxy-1-propyn-1-yl)-4,4,5,5-tetramethyl-(1,3,2)dioxaborolane

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:634196-63-7 SDS

634196-63-7Relevant academic research and scientific papers

Cobalt(I)-mediated preparation of polyborylated cyclohexadienes: Scope, limitations, and mechanistic insight

Geny, Anais,Lebaeuf, David,Rouquie, Gabriel,Vollhardt, K. Peter C.,Malacria, Max,Gandon, Vincent,Aubert, Corinne

, p. 5408 - 5425 (2008/03/12)

A series of 1,3- and 1,4-di-boryl-1,3-cyclohexadiencs have been prepared by intermolecular CoCp-mediated [2+2+2] cocyclizations of alkynylboronic pinacolate esters with alkenes, followed by oxidative demetallation with iron(III) chloride. The effect of su

Boron-directed regio- and stereoselective enyne cross metathesis: Efficient synthesis of vinyl boronate containing 1,3-dienes

Kim, Mansuk,Lee, Daesung

, p. 1865 - 1868 (2007/10/03)

(Chemical Equation Presented) Regio- and stereoselective enyne cross metathesis reactions between borylated alkynes and terminal alkenes were realized to provide a variety of functionalized vinyl boronates. High chemical yield and regioselectivity was ach

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