1185756-83-5 Usage
Uses
Used in Chemical Synthesis:
[(3R)-tetrahydrofuran-3-yl]ammonium chloride is utilized as a reactant in organic synthesis, playing a crucial role in the formation of complex molecular structures. Its ability to act as a nucleophilic catalyst in chemical reactions, such as alkylation, acylation, and condensation processes, enhances the efficiency and selectivity of these reactions.
Used in Pharmaceutical Synthesis:
[(3R)-tetrahydrofuran-3-yl]ammonium chloride serves as a key precursor in the synthesis of pharmaceutical compounds, contributing to the development of novel drugs and therapeutic agents. Its unique chemical properties enable the creation of diverse medicinal molecules with potential applications in various healthcare sectors.
Used in Phase-Transfer Catalysis:
[(3R)-tetrahydrofuran-3-yl]ammonium chloride is employed as a phase-transfer catalyst, facilitating reactions between compounds in different phases (e.g., solid-liquid, liquid-liquid). This function is particularly important in industrial processes where efficient mixing and reaction rates are essential for achieving desired product yields and purities.
Used in the Preparation of Other Ammonium Salts:
As a versatile quaternary ammonium salt, [(3R)-tetrahydrofuran-3-yl]ammonium chloride is also used as a starting material in the preparation of other ammonium salts. These salts find applications in various fields, including agriculture, water treatment, and the synthesis of ionic liquids.
Check Digit Verification of cas no
The CAS Registry Mumber 1185756-83-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,5,7,5 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1185756-83:
(9*1)+(8*1)+(7*8)+(6*5)+(5*7)+(4*5)+(3*6)+(2*8)+(1*3)=195
195 % 10 = 5
So 1185756-83-5 is a valid CAS Registry Number.
1185756-83-5Relevant academic research and scientific papers
Ramanujam, Rajendran,Ganjihal, Savita,Kalyanam, Nagabushanam,Majeed, Muhammed
, p. 663 - 668 (2013)
The synthesis of chemically and enantiomerically pure (S)-3-amino tetrahydrofuran hydrochloride starting from the natural amino acids, l-aspartic acid or l-methionine is described. The process involves no chromatography and can be easily carried out on a large scale. The enantiopurity of the final product was established by NMR and chiral HPLC methods.
Processes for the Manufacture of Chiral and Racemic Forms of 3-Aminotetrahydrofurans, Their Salts and Derivatives
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Page/Page column 4, (2008/12/04)
A novel process for the synthesis of (S)-3-Amino-tetrahydrofuran and (R)-3-Amino-tetrahydrofuran is described. The process is applicable for substituted chiral-3-aminotetrahydrofuran derivatives.
Novel compounds
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Page 80, (2008/06/13)
Novel substituted 2,4,8-trisubstituted-8H-pyrido[2,3-d]pyrimidin-7-one compounds and compositions for use in therapy as CSBP/p38 kinase inhibitors.
N6 mono heterocyclic substituted adenosine derivatives
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, (2008/06/13)
A substituted N 6 -oxa, thia, thioxa and azacycloalkyl substituted adenosine derivative and a method for using the composition as an A 1 heart adenosine receptor.
