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5-Cyanothiophene-2-boronic acid pinacol ester, with the chemical formula C12H15BClNO2S, is a boronic acid pinacol ester derivative of 5-cyanothiophene. It is a versatile building block in organic synthesis and medicinal chemistry, known for its high stability and compatibility with various reaction conditions. Its boron moiety enables cross-coupling reactions with other organic molecules, making it an essential tool for creating diverse chemical structures.

463336-26-7

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463336-26-7 Usage

Uses

Used in Pharmaceutical Industry:
5-Cyanothiophene-2-boronic acid pinacol ester is used as a key intermediate in the synthesis of various pharmaceuticals. Its ability to participate in cross-coupling reactions allows for the development of new drug candidates with unique chemical structures and potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, 5-cyanothiophene-2-boronic acid pinacol ester serves as a valuable building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its versatility in organic synthesis enables the creation of novel compounds with improved efficacy and selectivity in controlling pests and weeds.
Used in Materials Science:
5-Cyanothiophene-2-boronic acid pinacol ester is utilized in the development of advanced materials, such as organic semiconductors and optoelectronic devices. Its ability to form stable cross-coupled products with other organic molecules contributes to the design of materials with tailored electronic and optical properties.
Used in Chemical Research and Development:
As a stable and reactive boronic acid pinacol ester, 5-cyanothiophene-2-boronic acid pinacol ester is an important tool for chemical research and development. It facilitates the exploration of new synthetic routes, the discovery of novel chemical reactions, and the optimization of existing processes in various fields of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 463336-26-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,3,3,3 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 463336-26:
(8*4)+(7*6)+(6*3)+(5*3)+(4*3)+(3*6)+(2*2)+(1*6)=147
147 % 10 = 7
So 463336-26-7 is a valid CAS Registry Number.

463336-26-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene-3-carbonitrile

1.2 Other means of identification

Product number -
Other names -

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:463336-26-7 SDS

463336-26-7Downstream Products

463336-26-7Relevant academic research and scientific papers

Iridium-Catalyzed Silylation of Five-Membered Heteroarenes: High Sterically Derived Selectivity from a Pyridyl-Imidazoline Ligand

Hartwig, John F.,Karmel, Caleb,Kharitonova, Elena V.,Rubel, Camille Z.

supporting information, p. 6074 - 6081 (2020/02/25)

The steric effects of substituents on five-membered rings are less pronounced than those on six-membered rings because of the difference in bond angles. Thus, the regioselectivities of reactions of five-membered heteroarenes that occur with selectivities dictated by steric effects, such as the borylation of C?H bonds, have been poor in many cases. We report that the silylation of five-membered-ring heteroarenes occurs with high sterically derived regioselectivity when catalyzed by the combination of [Ir(cod)(OMe)]2 (cod=1,5-cyclooctadiene) and a phenanthroline ligand or a new pyridyl-imidazoline ligand that further increases the regioselectivity. The silylation reactions with these catalysts produce high yields of heteroarylsilanes from functionalization at the most sterically accessible C?H bonds of these rings under conditions that the borylation of C?H bonds with previously reported catalysts formed mixtures of products or products that are unstable. The heteroarylsilane products undergo cross-coupling reactions and substitution reactions with ipso selectivity to generate heteroarenes that bear halogen, aryl, and perfluoroalkyl substituents.

C-H Borylation Catalysts that Distinguish between Similarly Sized Substituents like Fluorine and Hydrogen

Miller, Susanne L.,Chotana, Ghayoor A.,Fritz, Jonathan A.,Chattopadhyay, Buddhadeb,Maleczka, Robert E.,Smith, Milton R.

supporting information, p. 6388 - 6392 (2019/08/26)

By modifying ligand steric and electronic profiles it is possible to C-H borylate ortho or meta to substituents in aromatic and heteroaromatic compounds, where steric differences between accessible C-H sites are small. Dramatic effects on selectivities between reactions using B2pin2 or 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (HBpin) are described for the first time. Judicious ligand and borane combinations give highly regioselective C-H borylations on substrates where typical borylation protocols afford poor selectivities.

Harnessing C-H Borylation/Deborylation for Selective Deuteration, Synthesis of Boronate Esters, and Late Stage Functionalization

Kallepalli, Venkata A,Gore, Kristin A.,Shi, Feng,Sanchez, Luis,Chotana, Ghayoor A.,Miller, Susanne L.,Maleczka, Robert E.,Smith, Milton R.

, p. 8341 - 8353 (2015/09/02)

Ir-catalyzed deborylation can be used to selectively deuterate aromatic and heteroaromatic substrates. Combined with the selectivities of Ir-catalyzed C-H borylations, uniquely labeled compounds can be prepared. In addition, diborylation/deborylation reactions provide monoborylated regioisomers that complement those prepared by C-H borylation. Comparisons between Ir-catalyzed deborylations and Pd-catalyzed deborylations of diborylated indoles described by Movassaghi are made. The Ir-catalyzed process is more effective for deborylating aromatics and is generally more effective in the monodeborylation of diborylated thiophenes. These processes can be applied to complex molecules such as clopidogrel.

Iridium-catalyzed borylation of thiophenes: versatile, synthetic elaboration founded on selective C-H functionalization

Chotana, Ghayoor A.,Kallepalli, Venkata A.,Maleczka Jr., Robert E.,Smith III, Milton R.

, p. 6103 - 6114 (2008/12/20)

Iridium-catalyzed borylation has been applied to various substituted thiophenes to synthesize poly-functionalized thiophenes in good to excellent yields. Apart from common functionalities compatible with iridium-catalyzed borylations, additional functional group tolerance to acyl (COMe) and trimethylsilyl (TMS) groups was also observed. High regioselectivities were observed in borylation of 3- and 2,5-di-substituted thiophenes. Electrophilic aromatic C-H/C-Si bromination on thiophene boronate esters is shown to take place without breaking the C-B bond, and one-pot C-H borylation/Suzuki-Miyaura cross-coupling has been accomplished on 2- and 3-borylated thiophenes.

Process for producing cyano substituted arene boranes and compounds

-

Page/Page column 21, (2008/06/13)

A process for producing cyano substituted arene boranes is described. The compounds are useful intermediates to pharmaceutical compounds using the cyano group as a reactant.

Synthesis of 2,3-Substituted Thienylboronic Acids and Esters

Christophersen, Claus,Begtrup, Mikael,Ebdrup, Soren,Petersen, Henning,Vedso, Per

, p. 9513 - 9516 (2007/10/03)

A noncryogenic protocol for the synthesis of 2-substituted 3-thienylboronic acids and esters as well as 3-substituted 2-thienylboronic acids and esters has been developed. Electrophiles were introduced regiospecifically in the 2-position of 2,3-dibromothiophene and in the 3-position of 2-bromo-3-iodothiophene by halogen-magnesium exchange followed by quenching with electrophiles. Palladium-catalyzed borylation of the 2,3-substituted halothiophenes with pinacolborane and P(t-Bu)3 as ligand for Pd produced 9 and 10. The borylation protocol was tolerated by a range of functional groups; however, strongly electron-withdrawing substituents decreased the stability of the thienylboronic acids and esters.

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