Category: 53636-17-2

Electric Literature of C5H13NO. Aromatic compounds can be divided into two categories: single heterocycles and fused heterocycles. Compound: (S)-1-(Dimethylamino)propan-2-ol, is researched, Molecular C5H13NO, CAS is 53636-17-2, about Rapid determination of enantiomeric excess using infrared thermography. Author is Millot, Nicolas; Borman, Phil; Anson, Mike S.; Campbell, Ian B.; Macdonald, Simon J. F.; Mahmoudian, Mahmoud.

IR thermog. (IRT) is presented as a novel technique to screen a potentially large number of asym. catalysts or substrates in a high-throughput fashion. IRT was used as a simple, rapid, and practical approach for initial screening of the substrate specificity of Candida antarctica lipase. This was carried out using a 96-well microtiter plate format. Potential advantages and limitations of IRT for the enzymic stereoselective acylation of primary and secondary alcs. of interest are discussed.

There is still a lot of research devoted to this compound(SMILES：C[C@H](O)CN(C)C)Electric Literature of C5H13NO, and with the development of science, more effects of this compound(53636-17-2) can be discovered.

Reference:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

HPLC of Formula: 53636-17-2. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: (S)-1-(Dimethylamino)propan-2-ol, is researched, Molecular C5H13NO, CAS is 53636-17-2, about Direct asymmetric aldol-Tishchenko reaction of aliphatic ketones catalyzed by syn-amino alcohol-Yb(III);complexes.

The asym. direct aldol condensation of aldehydes with ethyl- and Pr ketones is catalyzed by syn-α-amino alc.-Yb(OTf)3 complexes, yielding the anti-1,3-diol mono-esters with high diastereocontrol and good enantioselectivity. Three adjacent stereogenic centers are created in a simultaneous aldol condensation and Evans-Tishchenko reduction in an acyclic system.

There is still a lot of research devoted to this compound(SMILES：C[C@H](O)CN(C)C)HPLC of Formula: 53636-17-2, and with the development of science, more effects of this compound(53636-17-2) can be discovered.

Reference:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Synthesis of optically active methadones, LAAM and bufuralol by lipase-catalysed acylations, published in 2003-03-07, which mentions a compound: 53636-17-2, Name is (S)-1-(Dimethylamino)propan-2-ol, Molecular C5H13NO, Name: (S)-1-(Dimethylamino)propan-2-ol.

(R)- and (S)-Methadones and levo-α-acetylmethadol (LAAM) have been synthesized starting from lipase-catalyzed acylation of dimethylaminopropan-2-ol. An approach to the synthesis of (R)-bufuralol is also presented.

If you want to learn more about this compound((S)-1-(Dimethylamino)propan-2-ol)Name: (S)-1-(Dimethylamino)propan-2-ol, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(53636-17-2).

Reference:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Computed Properties of C5H13NO. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: (S)-1-(Dimethylamino)propan-2-ol, is researched, Molecular C5H13NO, CAS is 53636-17-2, about Direct enantiomeric separation of β-aminoalcohols with a tertiary amine moiety by ligand-exchange chromatography with chemiluminescence detection. Author is Yamazaki, Shigeo; Tanimura, Takenori; Uchikura, Kazuo.

Underivatized aliphatic β-aminoalcs. with a tertiary amine moiety could be separated into enantiomers by ligand-exchange chromatog. with chemiluminescence detection using octadecylsilanized silica gel coated with N-n-dodecyl-(1R,2S)-norephedrine as the stationary phase and an aqueous solution containing copper(II) and barbital as the mobile phase.

If you want to learn more about this compound((S)-1-(Dimethylamino)propan-2-ol)Computed Properties of C5H13NO, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(53636-17-2).

Reference:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 53636-17-2, is researched, Molecular C5H13NO, about Synthesis of tritium labeled choline analogs, the main research direction is choline tritiated; hydroxypropanyl ammonium iodide tritiated; propynyl ammonium iodide tritiated.Recommanded Product: (S)-1-(Dimethylamino)propan-2-ol.

(R)-(-)- And (S)-(+)-HOCHMeCH2N+Me2C3H3 I- were prepared from HOCHMeCH2NH2 by reductive methylation with CH2O and quaternization with C3H3I. (R)-(+)- And (S)-(-)-HOCH2CHMeN+Me2C3H3 I- and HCCCH2N+Me213CH3 I- were similarly prepared Radiochem. yields were ∼40%.

Here is a brief introduction to this compound(53636-17-2)Recommanded Product: (S)-1-(Dimethylamino)propan-2-ol, if you want to know about other compounds related to this compound(53636-17-2), you can read my other articles.

Reference:
Piperazine – Wikipedia,
Piperazines – an overview | ScienceDirect Topics