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1-(bromoethynyl)cyclohexene is a chemical compound characterized by the molecular formula C8H9Br. It is a highly reactive and potentially toxic compound that features a bromine atom and an ethynyl group attached to a cyclohexene ring. 1-(bromoethynyl)cyclohexene is known for its ability to participate in various chemical reactions, such as addition and substitution reactions, making it a valuable asset in organic synthesis and chemical research.

21983-34-6

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21983-34-6 Usage

Uses

Used in Organic Synthesis:
1-(bromoethynyl)cyclohexene is used as a key intermediate in organic synthesis for its reactivity and versatility in undergoing addition and substitution reactions. This allows for the creation of a wide range of complex organic molecules.
Used in Chemical Research:
In the field of chemical research, 1-(bromoethynyl)cyclohexene serves as a valuable compound for studying reaction mechanisms and exploring new synthetic pathways due to its unique structural features and reactivity.
Used in Pharmaceutical Production:
1-(bromoethynyl)cyclohexene is utilized as a building block in the production of various pharmaceuticals. Its ability to form different types of chemical bonds makes it a useful component in the synthesis of medicinal compounds.
Used in Agrochemical Production:
Similarly, in the agrochemical industry, 1-(bromoethynyl)cyclohexene is employed as a starting material for the synthesis of various agrochemicals, such as pesticides and herbicides, due to its potential to form a diverse array of chemical structures.
Safety Precautions:
It is crucial to handle 1-(bromoethynyl)cyclohexene with care, as it can be hazardous if not managed properly. Its high reactivity and potential toxicity necessitate proper safety measures, including the use of personal protective equipment and adherence to safety protocols, to minimize risks during its use in research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 21983-34-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,8 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 21983-34:
(7*2)+(6*1)+(5*9)+(4*8)+(3*3)+(2*3)+(1*4)=116
116 % 10 = 6
So 21983-34-6 is a valid CAS Registry Number.

21983-34-6SDS

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 1-(2-bromoethynyl)cyclohexene

1.2 Other means of identification

Product number -
Other names 1-bromoethynyl-cyclohexene

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:21983-34-6 SDS

21983-34-6Relevant academic research and scientific papers

Gold(I)-Catalyzed Oxidative 1,4-Additions of 3-En-1-ynamide with Nitrones via Carbon- versus Nitrogen-Addition Chemoselectivity

Tanpure, Sudhakar Dattatray,Kale, Balaji S.,Liu, Rai-Shung

, p. 1394 - 1399 (2021/02/20)

This work reports gold-catalyzed 1,4-oxofunctionalizations of 3-en-1-ynamides with nitrones, yielding two distinct E-configured products. We obtained 1,4-oxoarylation products from 3-en-1-ynamides bearing C(4)-electron-donating substituents and 1,4-oxoamination products from those analogues bearing C(4)-aryl substituents. We propose that if vinylgold carbenes are stable, imines undergo a para-arylation on these gold carbenes. If vinylgold carbenes are highly electron-deficient, this N-attack is irreversible to enable 1,4-oxoaminations.

Regio- and Stereoselective N-addition to an Open Bromo Vinyl Cation

Chuchmareva, Marina,Collong, Arndt,Niggemann, Meike,Schr?der, Sebastian,Strauch, Christina

supporting information, (2021/06/07)

A protocol for the synthesis of thus far inaccessible bromo vinyl triflimides is presented. Our previously reported concept of assisted vinyl cation formation was engaged to achieve both a protonation of relatively electron poor bromo alkynes and a reaction with high regio- and stereoselectivity. To the best of our knowledge, this is the first stereoselective addition of an N-nucleophile to an open β-halovinyl cation.

Dual Gold-Catalyzed Formal Tetradehydro-Diels–Alder Reactions for the Synthesis of Carbazoles and Indolines

Wang, Hong-Fa,Wang, Shi-Yue,Qin, Tian-Zhu,Zi, Weiwei

, p. 17911 - 17914 (2018/11/23)

This work reports a dual gold-catalyzed tetradehydro-Diels–Alder reaction for the synthesis of nitrogen-containing aromatic heterocycles. Under the catalytic system (IPrAuNTf2/DIPEA), indolines and carbazoles as well as other N-containing aromatic heterocycles were prepared in high yields with good functional group tolerance. Unlike the traditional thermal tetradehydro-Diels–Alder reactions, diluted reaction concentration and radical prohibitors are not required for this protocol. Experimental data support a mechanism involving gold vinylidene species, which undergoes a 6 π electrocyclization, followed with 1,2-hydrogen shift.

Borane-catalyzed selective hydrosilylation of internal ynamides leading to β-silyl (Z)-enamides

Kim, Youngchan,Dateer, Ramesh B.,Chang, Sukbok

supporting information, p. 190 - 193 (2017/11/27)

We have developed a borane-catalyzed regioand stereoselective hydrosilylation of internal ynamides for the first time. The scope of ynamide substrates and silane reactants was broad under mild reaction conditions, affording synthetically versatile β-silyl (Z)-enamide products. The observed stereoselectivity was reasoned to be due to the β-silicon effect on a postulated ketene iminium intermediate.

Gold-Catalyzed Intermolecular Ynamide Amination-Initiated Aza-Nazarov Cyclization: Access to Functionalized 2-Aminopyrroles

Shu, Chao,Wang, Yong-Heng,Shen, Cang-Hai,Ruan, Peng-Peng,Lu, Xin,Ye, Long-Wu

supporting information, p. 3254 - 3257 (2016/07/13)

A novel gold-catalyzed intermolecular ynamide amination-initiated aza-Nazarov cyclization has been developed, allowing the facile and efficient synthesis of various 2-aminopyrroles in moderate to good yields. Furthermore, a mechanistic rationale for this

Zinc-Catalyzed Stereo- and Regioselective 1,4-Hydrative Fluorination of 3-En-1-ynamides with Selectfluor

Jadhav, Appaso Mahadev,Huple, Deepak B.,Singh, Rahulkumar Rajmani,Liu, Rai Shung

supporting information, p. 1017 - 1022 (2016/04/19)

Zinc-catalyzed 1,4-oxofluorinations of 3-en-1-ynamides with Selectfluor in acetonitrile/water proceeded with high regio- and stereoselectivity, giving E-configured γ-fluoro-α,β-unsaturated amides efficiently. Our control experiments indicate that kinetica

Palladium-Catalyzed Regioselective Alkynylation of Pyrroles and Azoles under Mild Conditions: Application to the Synthesis of a Dopamine D-4 Receptor Agonist

Brachet, Etienne,Belmont, Philippe

, p. 7519 - 7529 (2015/08/18)

A mild and general method for the direct alkynylation of azoles such as pyrrole, indole, and 7-azaindole is described here. Using a simple catalytic system such as Pd(OAc)2 (2.5 mol %), P(tBu)2Me·HBF4 (5 mol %), and NaOAc (2 equiv) allowed the regioselective introduction of various alkynyl residues at the C-2 position of pyrroles. Interestingly, C-2 alkynylation was also observed on C-3-substituted indoles, whereas classical C-3 alkynylation was obtained on selected unsubstituted indoles and 7-azaindole. Our methodology has been illustrated by the efficient synthesis of a potential schizophrenia drug (dopamine D-4 inhibitor).

ZnII- and AuI-catalyzed regioselective hydrative oxidations of 3-En-1-ynes with selectfluor: Realization of 1,4-dioxo and 1,4-oxohydroxy functionalizations

Jadhav, Appaso Mahadev,Gawade, Sagar Ashok,Vasu, Dhananjayan,Dateer, Ramesh B.,Liu, Rai-Shung

, p. 1813 - 1817 (2014/03/21)

Catalytic 1,4-dioxo functionalizations of 3-en-1-ynes to (Z)- and (E)-2-en-1,4-dicarbonyl compounds are described. This regioselective difunctionalization was achieved in one-pot operation through initial alkyne hydration followed by in situ Selectfluor oxidation. The presence of pyridine alters the reaction chemoselectivity to give 4-hydroxy-2-en-1-carbonyl products instead. A cooperative action of pyridine and ZnII assists the hydrolysis of key oxonium intermediate.

Facile and efficient synthesis of 1-haloalkynes via DBU-mediated reaction of terminal alkynes and N-haloimides under mild conditions

Li, Mengru,Li, Yueju,Zhao, Baozhong,Liang, Fushun,Jin, Long-Yi

, p. 30046 - 30049 (2014/08/05)

Directly from terminal alkynes and with N-halosuccinimides (halo = Br and I) or N-cholorophthalimide as the halogen sources, DBU as the activator, 1-haloalkynes were prepared in good to excellent yields at room temperature. Bis(bromoalkyne) and bis(iodoal

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