Category: 19444-23-6

Stereospecific synthesis of chiral tertiary alkyl aryl ethers via Mitsunobu reaction with complete inversion of configuration was written by Shi, Yao-Jun;Hughes, David L.;McNamara, James M.. And the article was included in Tetrahedron Letters in 2003.Recommanded Product: 19444-23-6 This article mentions the following:

Mitsunobu reaction of (S)-EtCMe(OH)COOMe with 4-(benzyloxy)phenol provides (R)-4-PhCH₂OC₆H₄OCMeEtCOOMe in moderate yield at elevated temperatures (80-100鎺?. The S_N2 displacement pathway is evident by complete inversion of the (S)-alc. to the (R)-ether. Several analogous reactions were also performed. In the experiment, the researchers used many compounds, for example, Benzyl 2-hydroxy-2-methylpropanoate (cas: 19444-23-6Recommanded Product: 19444-23-6).

Benzyl 2-hydroxy-2-methylpropanoate (cas: 19444-23-6) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Recommanded Product: 19444-23-6

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Stereospecific synthesis of chiral tertiary alkyl aryl ethers via Mitsunobu reaction with complete inversion of configuration was written by Shi, Yao-Jun;Hughes, David L.;McNamara, James M.. And the article was included in Tetrahedron Letters in 2003.Recommanded Product: 19444-23-6 This article mentions the following:

Mitsunobu reaction of (S)-EtCMe(OH)COOMe with 4-(benzyloxy)phenol provides (R)-4-PhCH₂OC₆H₄OCMeEtCOOMe in moderate yield at elevated temperatures (80-100掳). The S_N2 displacement pathway is evident by complete inversion of the (S)-alc. to the (R)-ether. Several analogous reactions were also performed. In the experiment, the researchers used many compounds, for example, Benzyl 2-hydroxy-2-methylpropanoate (cas: 19444-23-6Recommanded Product: 19444-23-6).

Benzyl 2-hydroxy-2-methylpropanoate (cas: 19444-23-6) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Recommanded Product: 19444-23-6

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Stereospecific synthesis of chiral tertiary alkyl aryl ethers via Mitsunobu reaction with complete inversion of configuration was written by Shi, Yao-Jun;Hughes, David L.;McNamara, James M.. And the article was included in Tetrahedron Letters in 2003.Recommanded Product: 19444-23-6 This article mentions the following:

Mitsunobu reaction of (S)-EtCMe(OH)COOMe with 4-(benzyloxy)phenol provides (R)-4-PhCH₂OC₆H₄OCMeEtCOOMe in moderate yield at elevated temperatures (80-100°). The S_N2 displacement pathway is evident by complete inversion of the (S)-alc. to the (R)-ether. Several analogous reactions were also performed. In the experiment, the researchers used many compounds, for example, Benzyl 2-hydroxy-2-methylpropanoate (cas: 19444-23-6Recommanded Product: 19444-23-6).

Benzyl 2-hydroxy-2-methylpropanoate (cas: 19444-23-6) belongs to esters. Esters typically have a pleasant smell; those of low molecular weight are commonly used as fragrances and are found in essential oils and pheromones. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.Recommanded Product: 19444-23-6

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Versatile and Controlled Synthesis of Star and Branched Macromolecules by Dendritic Initiation was written by Trollsas, M.;Hedrick, J. L.;Mecerreyes, D.;Dubois, Ph.;Jerome, R.;Ihre, H.;Hult, A.. And the article was included in Macromolecules in 1997.Name: Benzyl 2-hydroxy-2-methylpropanoate This article mentions the following:

Multifunctional poly(caprolactones) with novel and well defined mol. architectures were synthesized by the use of new dendritic initiators. The ring-opening polymerization methods used to prepare these new structures allowed accurate control of mol. weight and narrow mol. weight distributions. In some cases, the new initiators enable deprotection in the α-position of the chain to produce new AB₂ macromonomers and their subsequent self-polymerization produces hyperbranched polyesters. The new polymers were characterized by ¹H-NMR, ¹³C-NMR and size exclusion chromatog. (SEC). ¹³C-NMR spectra clearly shows that the initiators are fully substituted to give polymers with two, four and six arms. In the experiment, the researchers used many compounds, for example, Benzyl 2-hydroxy-2-methylpropanoate (cas: 19444-23-6Name: Benzyl 2-hydroxy-2-methylpropanoate).

Benzyl 2-hydroxy-2-methylpropanoate (cas: 19444-23-6) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits, including apples, durians, pears, bananas, pineapples, and strawberries. Esterification is the general name for a chemical reaction in which two reactants (typically an alcohol and an acid) form an ester as the reaction product. Esters are common in organic chemistry and biological materials.Name: Benzyl 2-hydroxy-2-methylpropanoate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics

Spatial action of mosquito repellents was written by Schreck, Carl E.;Gilbert, Irwin H.;Weidhaas, D. E.;Posey, Kenneth H.. And the article was included in Journal of Economic Entomology in 1970.Name: Benzyl 2-hydroxy-2-methylpropanoate This article mentions the following:

The spatial action for selected repellents to Aedes aegypti (mosquito) was studied in an olfactometer. Of 44 compounds evaluated, all but 1 significantly reduced the approach of mosquitoes to within 15 in. of treated hands; 16 caused outstanding reduction of approach. In the experiment, the researchers used many compounds, for example, Benzyl 2-hydroxy-2-methylpropanoate (cas: 19444-23-6Name: Benzyl 2-hydroxy-2-methylpropanoate).

Benzyl 2-hydroxy-2-methylpropanoate (cas: 19444-23-6) belongs to esters. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Liquid esters of low volatility serve as softening agents for resins and plastics. Esters also include many industrially important polymers. Polymethyl methacrylate is a glass substitute sold under the names Lucite and Plexiglas; polyethylene terephthalate is used as a film (Mylar) and as textile fibres sold as Terylene, Fortrel, and Dacron.Name: Benzyl 2-hydroxy-2-methylpropanoate

Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics