Home Other Building Blocks (2R,3S)-2-Aminobutane-1,3-diol

(2R,3S)-2-Aminobutane-1,3-diol

CAS No.:
108102-48-3
Catalog Number:
AG0083XZ
Molecular Formula:
C4H11NO2
Molecular Weight:
105.1356
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
100mg
≥ 98%
1 week
United States
$118
- +
250mg
≥ 98%
1 week
United States
$184
- +
1g
≥ 98%
1 week
United States
$330
- +
5g
≥ 98%
1 week
United States
$1427
- +
Product Description
Catalog Number:
AG0083XZ
Chemical Name:
(2R,3S)-2-Aminobutane-1,3-diol
CAS Number:
108102-48-3
Molecular Formula:
C4H11NO2
Molecular Weight:
105.1356
MDL Number:
MFCD00672370
IUPAC Name:
(2R,3S)-2-aminobutane-1,3-diol
InChI:
InChI=1S/C4H11NO2/c1-3(7)4(5)2-6/h3-4,6-7H,2,5H2,1H3/t3-,4+/m0/s1
InChI Key:
MUVQIIBPDFTEKM-IUYQGCFVSA-N
SMILES:
OC[C@H]([C@@H](O)C)N
Properties
Complexity:
49  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Defined Bond Stereocenter Count:
0
Exact Mass:
105.079g/mol
Formal Charge:
0
Heavy Atom Count:
7  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
105.137g/mol
Monoisotopic Mass:
105.079g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
66.5A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-1.6  
Literature
Title Journal
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Bulge-like asymmetric heterodye clustering in DNA duplex results in efficient quenching of background emission based on the maximized excitonic interaction. Chemistry (Weinheim an der Bergstrasse, Germany) 20120827
Synthesis of oligonucleotides carrying thiol groups using a simple reagent derived from threoninol. Molecules (Basel, Switzerland) 20120824
Quencher-free molecular beacon tethering 7-hydroxycoumarin detects targets through protonation/deprotonation. Bioorganic & medicinal chemistry 20120715
Nick sealing by T4 DNA ligase on a modified DNA template: tethering a functional molecule on D-threoninol. Chemistry (Weinheim an der Bergstrasse, Germany) 20110905
Preparation of photoresponsive DNA tethering ortho-methylated azobenzene as a supra-photoswitch. Current protocols in nucleic acid chemistry 20110901
Synthesis and structural properties of oligonucleotides covalently linked to acridine and quindoline derivatives through a threoninol linker. Bioorganic & medicinal chemistry 20101101
Unexpectedly stable artificial duplex from flexible acyclic threoninol. Journal of the American Chemical Society 20101027
Positively charged base surrogate for highly stable 'base pairing' through electrostatic and stacking interactions. Journal of the American Chemical Society 20090729
Dye labelling of nucleosides. Chemical biology & drug design 20090401
Modulation of pK(a) of Brooker's merocyanine by DNA hybridization. Bioconjugate chemistry 20090201
In-stem molecular beacon containing a pseudo base pair of threoninol nucleotides for the removal of background emission. Angewandte Chemie (International ed. in English) 20090101
Spectroscopic labeling of A, S/T in the 1H-15N HSQC spectrum of uniformly (15N-13C) labeled proteins. Journal of magnetic resonance (San Diego, Calif. : 1997) 20081001
Threoninol as a scaffold of dyes (threoninol-nucleotide) and their stable interstrand clustering in duplexes. Organic & biomolecular chemistry 20080821
Preparation of coherent hetero clusters with threoninol scaffold. Nucleic acids symposium series (2004) 20080101
Incorporation of cationic dyes into DNA for distinct stabilization of duplex. Nucleic acids symposium series (2004) 20080101
Properties