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2-Butynoic acid, 4-phenoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32978-41-9

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32978-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32978-41-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,9,7 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 32978-41:
(7*3)+(6*2)+(5*9)+(4*7)+(3*8)+(2*4)+(1*1)=139
139 % 10 = 9
So 32978-41-9 is a valid CAS Registry Number.

32978-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenoxybut-2-ynoic acid

1.2 Other means of identification

Product number -
Other names 2-Butynoic acid,4-phenoxy

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:32978-41-9 SDS

32978-41-9Relevant academic research and scientific papers

Method for synthesizing acetylenic acid by using terminal alkyne and carbon dioxide

-

Paragraph 0178-0186, (2021/07/24)

The invention belongs to the field of organic synthesis, and particularly relates to a method for synthesizing acetylenic acid by using terminal alkyne and carbon dioxide. The method comprises the experimental steps that alkyne, alkali and a solvent are added into a reaction tube, the alkyne serves as a raw material, the alkali and the solvent provide a strong alkaline environment, CO2 is introduced into a reaction container to form a carbon dioxide atmosphere, heating and stirring reaction are carried out, after the reaction is finished, cooling is carried out to the room temperature, extraction and liquid separation are carried out, a water layer is acidified, then separation and purification are further carried out, and the acetylenic acid compound is obtained. The method is carried out under the conditions of low temperature and normal pressure, does not need to add a metal catalyst, is single in product and convenient to separate, good in substrate applicability and safe and simple to operate, and has potential industrial application prospects and good economic benefits.

Carboxylation of terminal alkynes with CO2 using novel silver N-heterocyclic carbene complexes

Li, Shanshan,Sun, Jing,Zhang, Zhizhi,Xie, Ruixia,Fang, Xiangchen,Zhou, Mingdong

, p. 10577 - 10584 (2016/07/07)

Four novel N-heterocyclic carbene (NHC) silver complexes, I-IV, have been synthesized and characterized. The single X-ray crystal diffraction data indicate a dinuclear solid-state structure for I and III and a mononuclear structure for II and IV. These complexes have been successfully used as efficient catalysts for the C-H activating carboxylation of terminal alkynes with CO2. A wide range of substrates with various functional groups afforded the corresponding aryl or alkyl substituted propiolic acids in good yields under mild conditions. Moreover, the role of bases and the reaction mechanism is thoroughly discussed.

Carbon dioxide capture and use: Organic synthesis using carbon dioxide from exhaust gas

Kim, Seung Hyo,Kim, Kwang Hee,Hong, Soon Hyeok

supporting information, p. 771 - 774 (2014/01/23)

A carbon capture and use (CCU) strategy was applied to organic synthesis. Carbon dioxide (CO2) captured directly from exhaust gas was used for organic transformations as efficiently as hyper-pure CO2 gas from a commercial source, even for highly air- and moisture-sensitive reactions. The CO2 capturing aqueous ethanolamine solution could be recycled continuously without any diminished reaction efficiency. Exhaust gas is good enough! Carbon dioxide captured directly from exhaust gas was used for organic syntheses (see picture) as efficiently as hyper-pure CO2 gas from a commercial source, even for highly air- and moisture-sensitive reactions. The CO2 capturing aqueous ethanolamine solution could be recycled continuously without any diminished reaction efficiency. Copyright

Ligand-free Ag(I)-catalyzed carboxylation of terminal alkynes with CO 2

Zhang, Xiao,Zhang, Wen-Zhen,Ren, Xiang,Zhang, Lin-Lin,Lu, Xiao-Bing

supporting information; experimental part, p. 2402 - 2405 (2011/06/25)

Chemical equations presented. A convenient approach to selectively prepare a wide range of functionalized propiolic acids was developed by AgI-catalyzed carboxylation of terminal alkynes using carbon dioxide as carboxylative agent under ligand-free conditions.

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