17016-87-4 Usage
Uses
Used in Organic Synthesis:
L-Leucinol hydrochloride is used as a chiral building block for the synthesis of various organic compounds. Its unique structure allows for the creation of enantiomerically pure products, which is crucial in the development of pharmaceuticals and other chiral molecules.
Used in Pharmaceutical Production:
L-Leucinol hydrochloride is utilized as a reagent in the production of pharmaceuticals. Its ability to create enantiomerically pure compounds makes it an essential component in the synthesis of chiral drugs, ensuring the desired biological activity and minimizing potential side effects.
Used in Chiral Separations:
L-Leucinol hydrochloride is used as a resolving agent in chiral separations. It helps in the separation of enantiomers, which is vital for the development of pure chiral compounds with specific biological activities.
Used in Catalytic Asymmetric Synthesis:
L-Leucinol hydrochloride is employed as a ligand in catalytic asymmetric synthesis. Its chiral properties enable the selective formation of enantiomerically pure products, improving the efficiency and selectivity of chemical reactions.
Used in Synthesis of Bioactive Compounds:
L-Leucinol hydrochloride is studied for its potential use as a chiral auxiliary in the synthesis of bioactive compounds. Its ability to induce chirality in the products can lead to the development of new pharmaceuticals and other bioactive molecules with specific therapeutic properties.
Used in Development of New Materials:
L-Leucinol hydrochloride is also considered as a component in the development of new materials. Its chiral nature and versatile chemical properties can contribute to the creation of innovative materials with unique properties and applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 17016-87-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,0,1 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17016-87:
(7*1)+(6*7)+(5*0)+(4*1)+(3*6)+(2*8)+(1*7)=94
94 % 10 = 4
So 17016-87-4 is a valid CAS Registry Number.
17016-87-4Relevant academic research and scientific papers
One-pot synthesis and biological and catalytic applications of organometallic complexes involving oxazolines and (R)/(S)-a-phenylethylamine
Luo, Mei,Li, Hong Mei
, p. 963 - 971 (2019/12/24)
The crystal structures of zinc complexes 1 and 3 were determined following synthesis via a one-pot method involving the reaction of 2-hydro-6-methyl-nicotinonitrile and 2-cyanopyridine with different l-amino alcohols mediated by 120–130?mol% ZnCl2/s
Synthesis method of chiral (S)-leucinol hydrochloride
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Paragraph 0006; 0008; 0009, (2016/11/17)
The invention provides chiral (S)-leucinol hydrochloride. The chemical formula of the chiral (S)-leucinol hydrochloride is shown in the description. A synthesis method of the chiral (S)-leucinol hydrochloride includes synthesis and separation; according to synthesis, after (S)-leucinol and manganese(II) chloride react in an anhydrous methanol solution for 40 hours, a solvent is removed in a rotating mode, dark red solid is obtained, trichloromethane and ethyl alcohol are then added for dissolution, and the product chiral (S)-leucinol hydrochloride is obtained after natural volatilization.
Renin Inhibitors. Substitution of the Leucyl Residues of Leu-Leu-Val-Phe-OCH3 with 3-Amino-2-hydroxy-5-methylhexanoic Acid
Johnson, Rodney L.
, p. 605 - 610 (2007/10/02)
The 2S,3S and 2R,3S diastereoisomers of the hydroxy amino acid 3-amino-2-hydroxy-5-methylhexanoic acid (AHMHA) were synthesized and substituted for the leucyl residues of Leu-Leu-Val-Phe-OCH3 to yield the following analogues: AHMHA-Leu-Val-Phe-OCH3, AHMHA
