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CAS No:2749-11-3
MF:C3H9NO
Appearance:colorless or light-yellow transparent liquid
Specification:98.5%
UN number:-
Package:1/5/10/25kgs/drum
Supply Capacity:MT
Synonyms:H-L-ALA-OL;H-ALANINOL;H-ALA-OL;H-ALA-OL S-(+)-2 AMINO-PROPANOL;L-(+)-ALANINOL;L-ALANINOL;L-ALANILOL;L-(+)-2-AMINO PROPANOL; L-Alaninol; 2749-11-3; (S)-2-Aminopropan-1-ol; 1-Propanol, 2-amino-, (2S)-; 2-Aminopropanol, (+)-; S-(+)-ALANINOL; V403GH89L1; L-2-AMINOPROPANOL; UNII-V403GH89L1; CHEBI:78502; EINECS 220-388-7; ((S)-1-(HYDROXYMETHYL)ETHYL)AMINE; L-2-AMINO-1-PROPANOL; RefChem:151792; 220-388-7; (S)-(+)-2-Amino-1-propanol; (2S)-2-aminopropan-1-ol; Alaninol; MFCD00064412; S-(+)-2-Amino-1-propanol; L-Ala-ol; (S)-2-amino-1-propanol; (+)-2-Aminopropan-1-ol; (2S)-2-amino-1-propanol; (S)-alaninol; (2S)-(+)-2-aminopropan-1-ol; M03438; L-2-aminopropan-1-ol; (+)-2-aminopropanol; (S)-2-amino-propan-1-ol; (S)-2-aminopropane-1-ol; Ala-ol; 2A1; (s)-2-aminopropanol; (S)-2-amino propanol; (S)-2-amino-propanol; (S)-2-aminopropan-1ol; (5)-2-aminopropan-1-ol; SCHEMBL72189; 2-(S)-amino-propan-1-ol; (25)-2-amino-1-propanol; (S)-1-hydroxymethylethylamine; SCHEMBL752373; orb2901436; CHEMBL1229871; SCHEMBL16500073; SCHEMBL30417235; (S)-(+) 2-amino-1-propanol; (S)-(+)-2 amino-1-propanol; (S)-(+)-2-aminopropan-1-ol; (S)-(-)-2-amino-1-propanol; DTXSID901347737; (S)-(+)-2-amino-propan-1-ol; CS-B1303; HY-Y0837; AKOS000302243; AC-1565; EBC-249063; FA47601; 40898-94-0; AC-24154; AS-12033; A1085; A4402; EN300-86282; A-4550; T27792; Q27147838; F0001-2971
Product application:L-Alaninol,(S)-2-Aminopropan-1-ol,L-2-Aminopropanol,(S)-(+)-2-Amino-1-propanol,L-Alaninol CAS 2749-11-3,high purity L-Alaninol,pharmaceutical grade L-Alaninol,L-Alaninol manufacturer,L-Alaninol supplier,chiral amino alcohol,chiral intermediate,chiral building block,chiral ligand precursor,asymmetric synthesis reagent,Ofloxacin intermediate,Levofloxacin synthesis intermediate,chiral oxazoline ligand,stereoselective synthesis block,chiral resolution agent,enantiopure L-Alaninol,bulk L-Alaninol price,chemical raw materials,amino alcohol intermediate,asymmetric catalytic synthesis中文SEO规范设置
L-Alaninol serves as an essential, high-value chiral building block derived from natural amino acid reduction, featuring dual-functional primary amino and hydroxyl moieties with exceptional stereochemical stability. It is predominantly utilized as a key chiral precursor in the pharmaceutical industry for synthesizing advanced fluoroquinolone antibiotics, active pharmaceutical ingredients (APIs), and therapeutic derivatives. In asymmetric synthesis and catalytic engineering, it plays an indispensable role in developing chiral oxazoline ligands, organocatalysts, and resolution auxiliaries. Furthermore, it finds extensive application in the stereoselective synthesis of specialty agrochemicals, advanced performance polymers, and fine chemical derivatives requiring rigorous enantiomeric purity.