133522-38-0 Usage
Uses
Used in Pharmaceutical Synthesis:
(S)-1-Amino-3-phenylpropan-2-ol is used as a key intermediate in the synthesis of various pharmaceuticals and organic compounds. Its unique structure and functional groups make it a valuable building block for the development of new drugs.
Used in Pain Management:
(S)-1-Amino-3-phenylpropan-2-ol is used as an analgesic agent for the management of pain. Its ability to alleviate pain makes it a potential candidate for the development of new pain-relieving medications.
Used in Anti-Inflammatory Applications:
(S)-1-Amino-3-phenylpropan-2-ol is used as an anti-inflammatory agent to reduce inflammation and associated symptoms. Its anti-inflammatory properties make it a promising compound for the development of new treatments for inflammatory conditions.
Used in Parkinson's Disease Treatment:
(S)-1-Amino-3-phenylpropan-2-ol is being studied for its potential role in the treatment of Parkinson's disease. Its ability to modulate certain pathways involved in the disease may lead to the development of new therapeutic strategies for Parkinson's patients.
Used in Organic Chemistry Reactions:
(S)-1-Amino-3-phenylpropan-2-ol is used as a valuable intermediate in various organic chemistry reactions. Its unique structure and functional groups make it a versatile compound for the synthesis of a wide range of organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 133522-38-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,5,2 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 133522-38:
(8*1)+(7*3)+(6*3)+(5*5)+(4*2)+(3*2)+(2*3)+(1*8)=100
100 % 10 = 0
So 133522-38-0 is a valid CAS Registry Number.
133522-38-0Relevant articles and documents
Rearrangement of N-alkyl 1,2-amino alcohols. Synthesis of (S)-toliprolol and (S)-propanolol
Duthion, Béranger,Métro, Thomas-Xavier,Gomez Pardo, Domingo,Cossy, Janine
experimental part, p. 6696 - 6706 (2011/02/26)
N-alkyl 1,2-amino alcohols were rearranged stereospecifically by using TFAA/Et3N. This rearrangement has been used to synthesize N-isopropyl-3-(aryloxy)-2-hydroxypropylamines, β-adrenergic blocking agents such as (S)-toliprolol and (S)-propanolol.
Synthesis of Peptidosulfinamides and Peptidosulfonamides: Peptidomimetics Containing the Sulfinamide or Sulfonamide Transition-State Isostere
Moree, Wilna J.,Marel, Gijs A. van der,Liskamp, Rob J.
, p. 5157 - 5169 (2007/10/02)
Synthetic routes are described toward the preparation of α- as well as β-substituted aminoethanesulfinyl chlorides, starting from either an aldehyde or from an amino acid derivative.The sulfinyl chlorides are used as building blocks for the preparation of homochiral α- or β-substituted sulfinamide and sulfonamide transition-state isosteres.The methodology has been applied to the synthesis of peptidosulfonamide peptidomimetics such as a hapten needed for the generation of antibodies and potential HIV protease inhibitors.In addition, the β-substituted aminoethanesulfinyl chlorides were used as building blocks for the preparation of a tetrapeptidosulfonamide, which can be considered as a biopolymer mimetic, employing a repetition of a cycle of three reactions: coupling of the sulfinyl chloride to the N-terminus of the growing peptidosulfonamide, oxidation to the sulfonamide, and deprotection of the N-terminus.
