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3-Butenoic acid Sale

(Synonyms: 乙烯基乙酸; Vinylacetic acid) 目录号 : GC61720

3-Butenoicacid(Vinylaceticacid)可用于合成双环3,6-dihydro-1,2-oxazine。应变双环3,6-dihydro-1,2-oxazine是多米诺复分解反应中与外部烯烃反应的底物。

3-Butenoic acid Chemical Structure

Cas No.:625-38-7

规格 价格 库存 购买数量
500 mg
¥450.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

3-Butenoic acid (Vinylacetic acid) can be used to synthesize bicyclic 3,6-dihydro-1,2-oxazine. Strained bicyclic 3,6-dihydro-1,2-oxazine is a reactive substrate in domino metathesis with an external alkene[1][2].

[1]. GÉraldine Calvet, et al. Domino metathesis of 3,6-dihydro-1,2-oxazine: access to isoxazolo[2,3-a]pyridin-7-ones. Org Lett. 2007 Apr 12;9(8):1485-8. [2]. M A Casado-Rodriguez, et al. Synthesis of vinyl-terminated Au nanoprisms and nanooctahedra mediated by 3-butenoic acid: direct Au@pNIPAM fabrication with improved SERS capabilities. Nanoscale. 2016 Feb 28;8(8):4557-64.

Chemical Properties

Cas No. 625-38-7 SDF
别名 乙烯基乙酸; Vinylacetic acid
Canonical SMILES C=CCC(O)=O
分子式 C4H6O2 分子量 86.09
溶解度 DMSO : 100 mg/mL (1161.58 mM; Need ultrasonic) 储存条件 Store at -20°C
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1 mg 5 mg 10 mg
1 mM 11.6158 mL 58.0788 mL 116.1575 mL
5 mM 2.3232 mL 11.6158 mL 23.2315 mL
10 mM 1.1616 mL 5.8079 mL 11.6158 mL
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Research Update

Palladium-Catalyzed Direct C-H Arylation of 3-Butenoic acid Derivatives

Org Lett 2021 Jan 15;23(2):296-299.PMID:33370124DOI:10.1021/acs.orglett.0c03773.

We report herein a direct method to synthesize 4-aryl-3-butenoic acid through a carboxylic-acid-directed oxidative Heck reaction. The various 4-aryl-3-butenoic acids are easily prepared in moderate to good yields. In view of the promising bioactivity of 4-phenyl-3-butenoic acid previously reported, its derivatives reported here may be bioactive.

Synthesis of vinyl-terminated Au nanoprisms and nanooctahedra mediated by 3-Butenoic acid: direct Au@pNIPAM fabrication with improved SERS capabilities

Nanoscale 2016 Feb 28;8(8):4557-64.PMID:26822759DOI:10.1039/c5nr08054a.

Here we describe the first seedless synthesis of vinyl-terminated Au nanotriangular prisms (AuNTPs) and nanooctahedra (AuNOC) in aqueous media. This synthesis is performed by chemical reduction of chloroauric acid (HAuCl4) with 3-Butenoic acid (3BA) in the presence of benzyldimethylammonium chloride (BDAC). The principal novelties of the presented method are the use of a mixture of 3BA and BDAC, the synthesis of gold prisms and octahedra with controllable size, and the presence of terminal double bonds on the metal surface. Initially this method produces a mixture of triangular gold nanoprisms and octahedra; however, both morphologies are successfully separated by surfactant micelle induced depletion interaction, reaching percentages up to ∼90%. Moreover, the alkene moieties present on the gold surface are exploited for the fabrication of hybrid core@shell particles. Gold octahedra and triangular prisms are easily encapsulated by free radical polymerization of N-isopropylacrylamide (NIPAM). Finally, in order to obtain a gold core with the most number of tips, AuNTP@pNIPAM microgels were subjected to gold core overgrowth, thus resulting in star-shaped nanoparticles (AuSTs@pNIPAM). We use 4-amino-benzenethiol as the model analyte for SERS investigations. As expected, gold cores with tips and high curvature sites produced the highest plasmonic responses.