150-05-0 Usage
Description
(S)-4-[1-hydroxy-2-(methylamino)ethyl]pyrocatechol is a complex organic compound with a unique molecular structure. It is characterized by its pyrocatechol core, which is a type of dihydroxybenzene, and a methylaminoethyl side chain attached to the 2nd carbon. The stereochemistry of the compound is defined by the "S" configuration, which indicates the spatial arrangement of the atoms in the molecule. (S)-4-[1-hydroxy-2-(methylamino)ethyl]pyrocatechol has potential applications in various fields due to its unique properties and reactivity.
Uses
Used in Pharmaceutical Industry:
(S)-4-[1-hydroxy-2-(methylamino)ethyl]pyrocatechol is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity make it a valuable building block for the development of new drugs with specific therapeutic properties.
Used in Chemical Research:
(S)-4-[1-hydroxy-2-(methylamino)ethyl]pyrocatechol is also used as a research tool in the field of organic chemistry. It can be employed to study the effects of stereochemistry on the reactivity and properties of molecules, as well as to explore new synthetic pathways and reaction mechanisms.
Used in Drug Delivery Systems:
(S)-4-[1-hydroxy-2-(methylamino)ethyl]pyrocatechol can be utilized in the development of drug delivery systems, where its unique structure and functional groups can be exploited to enhance the solubility, stability, and bioavailability of therapeutic agents.
Used in Analytical Chemistry:
The compound can also be used in analytical chemistry for the development of new methods and techniques for the detection and quantification of various substances, taking advantage of its unique chemical properties and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 150-05-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,5 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 150-05:
(5*1)+(4*5)+(3*0)+(2*0)+(1*5)=30
30 % 10 = 0
So 150-05-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H13NO3/c1-10-5-9(13)6-2-3-7(11)8(12)4-6/h2-4,9-13H,5H2,1H3/t9-/m1/s1
150-05-0Relevant articles and documents
In-situ and one-step preparation of protein film in capillary column for open tubular capillary electrochromatography enantioseparation
Li, Ling,Xue, Xuqi,Zhang, Huige,Lv, Wenjuan,Qi, Shengda,Du, Hongying,Manyande, Anne,Chen, Hongli
supporting information, p. 2139 - 2142 (2021/04/07)
In this work, the phase-transitioned BSA (PTB) film using the mild and fast fabrication process adhered to the capillary inner wall uniformly, and the fabricated PTB film-coated capillary column was applied to realize open tubular capillary electrochromatography (OT-CEC) enantioseparation. The enantioseparation ability of PTB film-coated capillary was evaluated with eight pairs of chiral analytes including drugs and neurotransmitters, all achieving good resolution and symmetrical peak shape. For three consecutive runs, the relative standard deviations (RSD) of migration time for intra-day, inter-day, and column-to-column repeatability were in the range of 0.3%–3.5%, 0.2%–4.9% and 2.1%–7.7%, respectively. Moreover, the PTB film-coated capillary column ran continuously over 300 times with high separation efficiency. Therefore, the coating method based on BSA self-assembly supramolecular film can be extended to the preparation of other proteinaceous capillary columns.
Electroreductive generation of (S)-(+)-N,N-dimethyl-2-(hydroxymethyl)- pyrrolidinium mercury compound for enantioselective synthesis of 2-amino-1-alkyl/aryl ethanols
Yadav, Ashok K.,Manju, Meera
, p. 2770 - 2772 (2008/04/18)
(S)-(+)-N, N - Dimethyl-2-(hydroxymethyl)-pyrrolidinium (DMHP +)-mercury compound mediated enantioselective reduction of aminomethyl alkyl/aryl ketones in dimethylformamide-2-propanol (9:1) has been carried out using tetrabutylammonium tetrafluoroborate as a supporting electrolyte. The products viz. 2-amino-1-alkyl/aryl ethanols have been obtained in good yield (68-92%) with 35-91% optical purity and have been assigned (S)-configuration. The pinacol (racemic/meso) derivatives are also isolated as minor products (yield 5-20%) via dimerization of radical anion followed by protonation.
