CHEMOS
Oligonucleotide Synthesis, RNA Raw Materials & Modification

L-Threoninol

(2R,3R)-2-aminobutane-1,3-diol

N° produitCH59016N° CAS3228-51-1Pureté99.5%
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Résumé du produit

Aperçu rapide

Famille de produits
Oligonucleotide Synthesis, RNA Raw Materials & Modification
Nom chimique
(2R,3R)-2-aminobutane-1,3-diol
FM
C4H11NO2
PM
105.14
Pureté
99.5%

L-Threoninol is a chiral amino alcohol identified as (2R,3R)-2-aminobutane-1,3-diol. It is also indexed as threoninol, H-threoninol, reduced threonine, and (2R,3R)-2-amino-1,3-butanediol.

CH59016 is listed with CAS 3228-51-1, molecular formula C4H11NO2, and molecular weight 105.14. Research literature links L-threoninol with acyclic L-threoninol nucleic acid scaffold chemistry, L-aTNA phosphoramidite monomer and chemical-ligation method studies, and chiral fluorescent recognition of threoninol.

Synonymes

Threoninol; H-Threoninol; Reduced Threonine; (2R,3R)-2-Amino-1,3-butanediol; 1,3-Butanediol, 2-amino-, (2R,3R)-

Identité et spécifications

Catalog No.CH59016
CAS No.3228-51-1
Molecular FormulaC4H11NO2
Molecular Weight105.14
PubChem CID2033049
InChIKeyMUVQIIBPDFTEKM-QWWZWVQMSA-N
Purity99.5%

Conditions de stockage

-20 C

Caractéristiques techniques

Scaffold class
Chiral amino diol
Stereochemistry
(2R,3R)
Functional groups
Primary amine and 1,3-diol
Research role
L-aTNA scaffold precursor
Grade
97% product designation
Packaging
1 g product code; Custom packaging on request
Physical form
Liquid

Contexte d’application

  • L-aTNA scaffold chemistry: reported in artificial nucleic acid studies involving acyclic L-threoninol nucleic acid cross-pairing with DNA and RNA.
  • Monomer and ligation methods: relevant to L-aTNA phosphoramidite monomer synthesis and chemical-ligation method research.
  • Chiral recognition: reported in fluorescent probe studies for selective recognition of threoninol.

Ressources techniques associées

Sources publiques

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