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Benzamide, 4-ethynyl(9CI) is a chemical compound characterized by the molecular formula C9H7NO. It features a benzamide ring with a distinctive 4-ethynyl substitution, which endows the compound with unique reactivity and properties. This makes it a valuable asset in the realm of organic synthesis, particularly for the preparation of pharmaceuticals and agrochemicals. Its potential as a building block in the development of novel materials and as a starting material in the synthesis of complex organic molecules further underscores its versatility and utility in organic chemistry.

90347-86-7

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90347-86-7 Usage

Uses

Used in Pharmaceutical Industry:
Benzamide, 4-ethynyl(9CI) serves as a crucial precursor in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, contributing to advancements in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, Benzamide, 4-ethynyl(9CI) is utilized as a starting material for the preparation of agrochemicals. Its reactivity and properties enable the creation of effective compounds for agricultural applications, such as pesticides and herbicides.
Used in Organic Synthesis:
Benzamide, 4-ethynyl(9CI) is employed as a versatile building block in the development of novel materials. Its unique reactivity allows for the synthesis of complex organic molecules, which can be used in a wide range of applications, from specialty chemicals to advanced materials.
Used in Research and Development:
Benzamide, 4-ethynyl(9CI)'s potential as a starting material in the synthesis of complex organic molecules makes it an invaluable tool for research and development in the field of organic chemistry. It facilitates the exploration of new chemical reactions and the discovery of innovative applications for organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 90347-86-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,3,4 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90347-86:
(7*9)+(6*0)+(5*3)+(4*4)+(3*7)+(2*8)+(1*6)=137
137 % 10 = 7
So 90347-86-7 is a valid CAS Registry Number.

90347-86-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-ethynylbenzamide

1.2 Other means of identification

Product number -
Other names 1-carboxamido-4-ethynylbenzene

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:90347-86-7 SDS

90347-86-7Relevant academic research and scientific papers

Visible light-mediated synthesis of amides from carboxylic acids and amine-boranes

Chen, Xuenian,Kang, Jia-Xin,Ma, Yan-Na,Miao, Yu-Qi

supporting information, p. 3595 - 3599 (2021/06/06)

Here, a photocatalytic deoxygenative amidation protocol using readily available amine-boranes and carboxylic acids is described. This approach features mild conditions, moderate-to-good yields, easy scale-up, and up to 62 examples of functionalized amides with diverse substituents. The synthetic robustness of this method was also demonstrated by its application in the late-stage functionalization of several pharmaceutical molecules.

PROCESS FOR HYDROCYANATION OF TERMINAL ALKYNES

-

, (2018/12/13)

The present invention refers to a process for a Rh-catalyzed Anti-Markovnikov hydrocyanation of terminal alkynes which process discloses, for the first time, the highly stereo- and regio-selective hydrocyanation of terminal alkynes to furnish E- configured alkenyl nitriles and the catalyst used in the present process.

Rh-Catalyzed Anti-Markovnikov Hydrocyanation of Terminal Alkynes

Ye, Fei,Chen, Junting,Ritter, Tobias

, p. 7184 - 7187 (2017/06/05)

We report the first highly stereo- and regioselective hydrocyanation of terminal alkynes to furnish E-configured alkenyl nitriles. Acrylonitriles can be accessed on gram scale with broad substrate scope and functional group tolerance. The hydrocyanation reaction employs acetone cyanohydrin as a practical alternative to HCN gas.

ALKYNYL PHOSPHINE GOLD COMPLEXES FOR TREATING BACTERIAL INFECTIONS

-

Page/Page column 83; 84, (2017/08/01)

A compound of formula (I) for use in the prevention or treatment of a bacterial infection.

NOVEL CONDENSED PYRAZOLE DERIVATIVE AND MEDICAL USES THEREOF

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Paragraph 0299; 0300; 0302; 0304, (2016/10/10)

PROBLEM TO BE SOLVED: To provide a preventive or therapeutic agent for mood disorder, anxiety disorder, schizophrenia, dementia, drug dependence or the like related to subtypes of metabolism type glutamate receptor (mGlu) 2 and 3. SOLUTION: There are prov

Design, Synthesis, and Evaluation of Triazole Derivatives That Induce Nrf2 Dependent Gene Products and Inhibit the Keap1-Nrf2 Protein-Protein Interaction

Bertrand, Hélène C.,Schaap, Marjolein,Baird, Liam,Georgakopoulos, Nikolaos D.,Fowkes, Adrian,Thiollier, Clarisse,Kachi, Hiroko,Dinkova-Kostova, Albena T.,Wells, Geoff

, p. 7186 - 7194 (2015/10/05)

The transcription factor Nrf2 regulates the expression of a large network of cytoprotective and metabolic enzymes and proteins. Compounds that directly and reversibly inhibit the interaction between Nrf2 and its main negative regulator Keap1 are potential pharmacological agents for a range of disease types including neurodegenerative conditions and cancer. We describe the development of a series of 1,4-diphenyl-1,2,3-triazole compounds that inhibit the Nrf2-Keap1 protein-protein interaction (PPI) in vitro and in live cells and up-regulate the expression of Nrf2-dependent gene products.

Transition-metal-free hydration of nitriles using potassium tert -butoxide under anhydrous conditions

Midya, Ganesh Chandra,Kapat, Ajoy,Maiti, Subhadip,Dash, Jyotirmayee

supporting information, p. 4148 - 4151 (2015/05/05)

Potassium tert-butoxide acts as a nucleophilic oxygen source during the hydration of nitriles to give the corresponding amides under anhydrous conditions. The reaction proceeds smoothly for a broad range of substrates under mild conditions, providing an efficient and economically affordable synthetic route to the amides in excellent yields. This protocol does not need any transition-metal catalyst or any special experimental setup and is easily scalable to bulk scale synthesis. A single-electron-transfer radical mechanism as well as an ionic mechanism have been proposed for the hydration process.

A general and efficient heterogeneous gold-catalyzed hydration of nitriles in neat water under mild atmospheric conditions

Liu, Yong-Mei,He, Lin,Wang, Miao-Miao,Cao, Yong,He, He-Yong,Fan, Kang-Nian

scheme or table, p. 1392 - 1396 (2012/10/07)

Mild, efficient and general: Titania decorated with nanometer-sized gold particles acts as an efficient catalyst for the selective hydration of a wide range of chemically diverse nitriles into valuable amides in neutral water, under mild atmospheric conditions (see image). The process shows promise for a facile and direct one-pot synthesis of ?μ-caprolactam, an industrially important molecule, starting from 6-aminocapronitrile. Copyright

Hammett analysis of selective thyroid hormone receptor modulators reveals structural and electronic requirements for hormone antagonists

Nguyen, Ngoc-Ha,Apriletti, James W.,Baxter, John D.,Scanlan, Thomas S.

, p. 4599 - 4608 (2007/10/03)

Selective thyroid hormone modulators that function as isoform-selective agonists or antagonists of the thyroid hormone receptors (TRs) might be therapeutically useful in diseases associated with aberrant hormone signaling. The most potent thyroid hormone

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