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4,4,5,5-Tetramethyl-2-((Z)-1-propenyl)-1,3,2-dioxaborolane, also known as cis-1-Propenylboronic acid pinacol ester, is a substituted alkylboronate compound with a unique structure that features a boron atom bonded to a dioxaborolane ring and a (Z)-1-propenyl group. 4,4,5,5-Tetramethyl-2-((Z)-1-propenyl)-1,3,2-dioxaborolane is known for its synthetic utility in the preparation of various pharmaceutical products.

83947-59-5

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83947-59-5 Usage

Uses

Used in Pharmaceutical Industry:
4,4,5,5-Tetramethyl-2-((Z)-1-propenyl)-1,3,2-dioxaborolane is used as a synthetic intermediate for the preparation of various pharmaceutical goods. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of a wide range of pharmaceutical compounds.
In the pharmaceutical industry, 4,4,5,5-Tetramethyl-2-((Z)-1-propenyl)-1,3,2-dioxaborolane is particularly useful for the synthesis of complex organic molecules, including those with potential therapeutic applications. Its ability to participate in various types of chemical reactions, such as Suzuki-Miyaura cross-coupling, allows for the efficient construction of diverse molecular frameworks that can be further optimized for specific biological targets.
Furthermore, the use of 4,4,5,5-Tetramethyl-2-((Z)-1-propenyl)-1,3,2-dioxaborolane in the synthesis of pharmaceuticals can lead to the development of new drugs with improved efficacy, safety, and pharmacokinetic properties. Its versatility and synthetic utility make it an important tool for medicinal chemists and drug developers in their quest to discover and create novel therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 83947-59-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,4 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83947-59:
(7*8)+(6*3)+(5*9)+(4*4)+(3*7)+(2*5)+(1*9)=175
175 % 10 = 5
So 83947-59-5 is a valid CAS Registry Number.

83947-59-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4,5,5-Tetramethyl-2-[(1Z)-1-propen-1-yl]-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names 4,4,5,5-tetramethyl-2-(prop-1-en-1-yl)-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:83947-59-5 SDS

83947-59-5Relevant academic research and scientific papers

(Z)-Selective Hydroboration of Terminal Alkynes Catalyzed by a PSP-Pincer Rhodium Complex

Lyu, Yanzong,Toriumi, Naoyuki,Iwasawa, Nobuharu

supporting information, p. 9262 - 9266 (2021/11/30)

A highly (Z)-selective hydroboration of terminal alkynes was achieved using a thioxanthene-based PSP-pincer rhodium catalyst. This hydroboration exhibited good chemoselectivity toward alkynes over carbonyl compounds such as ketones and aldehydes. The mechanistic studies indicated the involvement of rhodium-vinylidene intermediates, and the high (Z)-selectivity could be attributed to the rigid and electron-rich nature of the PSP-rhodium catalyst.

ISOMERIZATION OF ALKENES

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Page/Page column 20-21; 23, (2020/04/25)

The present invention relates to an isomerization method for alkenes, comprising of reaction an alkene with a Ni(I)-compound. By this method, E-Alkenes are obtained in excellent yield.

Ru-catalyzed isomerization of ω-alkenylboronates towards stereoselective synthesis of vinylboronates with subsequent: In situ functionalization

Ho, Guo-Ming,Marek, Ilan,Segura, Lucas

, p. 5944 - 5949 (2020/07/10)

The stereoselective preparation of synthetically versatile vinylboronates from ω-alkenylboronates is achieved through a ruthenium-catalyzed isomerization reaction. A variety of di- A nd trisubstituted vinylboronates were conveniently produced and could be

Stereoselective Bromoboration of Acetylene with Boron Tribromide: Preparation and Cross-Coupling Reactions of (Z)-Bromovinylboronates

Polá?ek, Jan,Paciorek, Jan,Sto?ek, Jakub,Semrád, Hugo,Munzarová, Markéta,Mazal, Ctibor

, p. 6992 - 7000 (2020/06/05)

The mechanism of acetylene bromoboration in neat boron tribromide was studied carefully by means of experiment and theory. Besides the syn-addition mechanism through a four-center transition state, radical and polar anti-addition mechanisms are postulated, both triggered by HBr, which is evidenced also to take part in the Z/E isomerization of the product. The proposed mechanism is well supported by ab initio calculations at the MP2/6-31+G? level with Ahlrichs' SVP all-electron basis for Br. Implicit solvation in CH2Cl2 has been included using the PCM and/or SMD continuum solvent models. Comparative case studies have been performed involving the B3LYP/6-31+G? with Ahlrichs' SVP for Br and MP2/Def2TZVPP levels. The mechanistic studies resulted in development of a procedure for stereoselective bromoboration of acetylene yielding E/Z mixtures of dibromo(bromovinyl)borane with the Z-isomer as a major product (up to 85%). Transformation to the corresponding pinacol and neopentyl glycol boronates and stereoselective decomposition of their E-isomer provided pure (Z)-(2-bromovinyl)boronates in 57-60% overall yield. Their reactivity in a Negishi cross-coupling reaction was tested. An example of the one-pot reaction sequence of Negishi and Suzuki-Miyaura cross-couplings for synthesis of combretastatin A4 is also presented.

Aliphatic α-Boryl-α-bromoketones: Synthesis and Reactivity

Ivon, Yevhen M.,Kuchkovska, Yuliya O.,Voitenko, Zoya V.,Grygorenko, Oleksandr O.

, p. 3367 - 3377 (2020/03/13)

A protocol for the preparation of α-boryl-α-bromoketones from alkenyl MIDA boronates was developed and applied to functionalized aliphatic derivatives. The reaction sequence included regioselective hydroxybromination of olefin moiety, followed by oxidation of alcohol group with Dess–Martin periodinane. The target trifunctional boronate-containing derivatives were obtained in up to 94 % yield over two steps starting from alkenyl MIDA boronates. In some cases, functional groups present in the substrate participated in the bromohydroxylation step via intramolecular nucleophilic attack at the bromonium cation leading to cyclic products. Additionally, the reactivity of aliphatic α-boryl-α-bromoketones was illustrated by nucleophilic substitution at the α-C atom and heterocyclization reactions.

E-Olefins through intramolecular radical relocation

Kapat, Ajoy,Sperger, Theresa,Guven, Sinem,Schoenebeck, Franziska

, p. 391 - 396 (2019/02/03)

Full control over the selectivity of carbon-carbon double-bond migrations would enable access to stereochemically defined olefins that are central to the pharmaceutical, food, fragrance, materials, and petrochemical arenas. The vast majority of double-bond migrations investigated over the past 60 years capitalize on precious-metal hydrides that are frequently associated with reversible equilibria, hydrogen scrambling, incomplete E/Z stereoselection, and/or high cost. Here, we report a fundamentally different, radical-based approach.We showcase a nonprecious, reductant-free, and atom-economical nickel (Ni)(I)-catalyzed intramolecular 1,3-hydrogen atom relocation to yield E-olefins within 3 hours at room temperature. Remote installations of E-olefins over extended distances are also demonstrated.

Enantioselective Conjunctive Cross-Coupling of Bis(alkenyl)borates: A General Synthesis of Chiral Allylboron Reagents

Edelstein, Emma K.,Namirembe, Sheila,Morken, James P.

supporting information, p. 5027 - 5030 (2017/05/04)

Palladium-catalyzed conjunctive cross-coupling is used for the synthesis of enantioenriched allylboron reagents. This reaction employs nonsymmetric bis(alkenyl)borates as substrates and appears to occur by a mechanism that involves selective activation of the less substituted alkene followed by migration of the more substituted alkene during the course of a Pd-induced metalate rearrangement.

Double-Bond Isomerization: Highly Reactive Nickel Catalyst Applied in the Synthesis of the Pheromone (9 Z,12 Z)-Tetradeca-9,12-dienyl Acetate

Weber, Felicia,Schmidt, Anastasia,R?se, Philipp,Fischer, Michel,Burghaus, Olaf,Hilt, Gerhard

supporting information, p. 2952 - 2955 (2015/06/30)

A highly reactive nickel catalyst comprising NiCl2(dppp) or NiCl2(dppe) with zinc powder, ZnI2 and Ph2PH, was applied in the isomerization of terminal alkenes to Z-2-alkenes. The double-bond geometry of the 2-alkene can be controlled via the reaction temperature to yield the 2-Z-alkenes in excellent yields and high Z-selectivities. The formation of other constitutional isomers, such as 3-alkenes, is suppressed on the basis of the proposed mechanism via a 1,2-hydride shift from the metal to the Ph2P ligand. The nickel-catalyzed isomerization reaction was then applied in the synthesis of (9Z,12Z)-tetradeca-9,12-dienyl acetate, a pheromone with a 2Z,5Z-diene subunit.

Enantioselective syn and anti homocrotylation of aldehydes: Application to the formal synthesis of spongidepsin

Lin, Hongkun,Tian, Leiming,Krauss, Isaac J.

supporting information, p. 13176 - 13182 (2015/10/28)

Whereas crotylboration has been a useful method for synthesis of stereochemically complex products, we have shown that homocrotylboration can be achieved with cyclopropanated crotylation reagents, and that the stereoselectivity of the reaction can be predicted by analogous models. This paper presents a full account of this work, including the first examples of asymmetric anti homocrotylation. The scope of this reaction is demonstrated with highly enantioselective homocrotylation of both aliphatic and aromatic aldehydes, as well as double diastereoselection studies. An application of the synthesis of the marine natural product spongidepsin is presented, as well as streamlined syntheses of homocrotylation reagents.

Enantiospecific, regioselective cross-coupling reactions of secondary allylic boronic esters

Chausset-Boissarie, Laetitia,Ghozati, Kazem,Labine, Emily,Chen, Jack L.-Y.,Aggarwal, Varinder K.,Crudden, Cathleen M.

supporting information, p. 17698 - 17701 (2014/01/17)

An original syn: The first enantioselective Suzuki-Miyaura cross-coupling of chiral, enantioenriched secondary allylic boronic esters is described (see scheme; DME=dimethoxyethane, Bpin = pinacolboryl, dba = dibenzylideneacetone). Mechanistic studies show that the reactions proceed via γ-selective transmetalation followed by reductive elimination. The reaction provides the first independent confirmation that the transmetalation of boronic esters proceeds via a syn pathway. Copyright

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