112150-28-4 Usage
Uses
Used in Pharmaceutical Research and Development:
(2S,3S)-3-Methyl-2-(MethylaMino)pentan-1-ol hydrochloride is used as a chiral building block in the synthesis of various pharmaceutical compounds. Its unique stereochemistry allows for the creation of enantiomerically pure drugs, which can have different biological activities and reduce potential side effects.
Used in Organic Synthesis:
In the field of organic synthesis, (2S,3S)-3-Methyl-2-(MethylaMino)pentan-1-ol hydrochloride serves as a valuable intermediate for the preparation of complex organic molecules. Its hydroxyl and methylamino functional groups can be further modified or used as starting points for the synthesis of a wide range of compounds, including pharmaceuticals, agrochemicals, and specialty chemicals.
Used in Laboratory and Industrial Applications:
The hydrochloride form of (2S,3S)-3-Methyl-2-(MethylaMino)pentan-1-ol enhances its solubility and stability, making it more suitable for use in various laboratory and industrial processes. This improved solubility can facilitate its incorporation into formulations, reactions, and other applications where a stable and soluble compound is required.
Check Digit Verification of cas no
The CAS Registry Mumber 112150-28-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,1,5 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112150-28:
(8*1)+(7*1)+(6*2)+(5*1)+(4*5)+(3*0)+(2*2)+(1*8)=64
64 % 10 = 4
So 112150-28-4 is a valid CAS Registry Number.
112150-28-4Relevant academic research and scientific papers
Aitali,Allaoud,Karim,Meliet,Mortreux
, p. 1367 - 1374 (2000)
The catalytic enantioselective reduction of aromatic ketones in 2- propanol is carried out by using ruthenium(II) complexes prepared from [Ru(p- cymene)Cl2]2 and a variety of chiral diamines and β-aminoalcohols derived from α-amino acids. Good conversions (>99%) and enantioselectivities (=96%) are observed under mild reaction conditions. (C) 2000 Elsevier Science Ltd.
SYNTHESE D'AMINOPHOSPHINEPHOSPHINITES CHIRAUX. UTILISATION EN REDUCTION ASYMETRIQUE CATALYTIQUE
Karim, A.,Mortreux, A.,Petit, F.,Buono, G.,Pfeiffer, G.,Siv, C.
, p. 93 - 104 (2007/10/02)
The chiral aminophosphinephosphinites ligands (AMPP) are directly synthesized from natural amino alcohols or by reduction of formyl esters of α-amino acids and PPh2Cl. Their cationic rhodium complexes have been found to be excellent catalysts for enantioselective hydrogenation of dehydroamino acids (ee ca. 86percent, yield ca. 100percent) for example.Asymmetric reduction of ketones can also be performed with the new alkyl AMPP* modified rhodium catalyst (ee 50percent).
