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73731-37-0

73731-37-0 | Fmoc-Thr-OH

CAS No: 73731-37-0 Catalog No: AG003QNM MDL No:MFCD00077072

Product Description

Catalog Number:
AG003QNM
Chemical Name:
Fmoc-Thr-OH
CAS Number:
73731-37-0
Molecular Formula:
C19H19NO5
Molecular Weight:
341.3579
MDL Number:
MFCD00077072
IUPAC Name:
(2S,3R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxybutanoic acid
InChI:
InChI=1S/C19H19NO5/c1-11(21)17(18(22)23)20-19(24)25-10-16-14-8-4-2-6-12(14)13-7-3-5-9-15(13)16/h2-9,11,16-17,21H,10H2,1H3,(H,20,24)(H,22,23)/t11-,17+/m1/s1
InChI Key:
OYULCCKKLJPNPU-DIFFPNOSSA-N
SMILES:
O=C(N[C@H](C(=O)O)[C@H](O)C)OCC1c2ccccc2c2c1cccc2

Properties

Complexity:
474  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Defined Bond Stereocenter Count:
0
Exact Mass:
341.126g/mol
Formal Charge:
0
Heavy Atom Count:
25  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Isotope Atom Count:
0
Molecular Weight:
341.363g/mol
Monoisotopic Mass:
341.126g/mol
Rotatable Bond Count:
6  
Topological Polar Surface Area:
95.9A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
2.4  

Literature

Title Journal
Synthesis of an Fmoc-threonine bearing core-2 glycan: a building block for PSGL-1 via Fmoc-assisted solid-phase peptide synthesis. Carbohydrate research 20100719
Exploiting enzymatic (reversed) hydrolysis in directed self-assembly of peptide nanostructures. Small (Weinheim an der Bergstrasse, Germany) 20080201
Total chemical synthesis and NMR characterization of the glycopeptide tx5a, a heavily post-translationally modified conotoxin, reveals that the glycan structure is alpha-D-Gal-(1-->3)-alpha-D-GalNAc. European journal of biochemistry 20041201
Practical synthesis of the 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-beta-D-glucosides of Fmoc-serine and Fmoc-threonine and their benzyl esters. Carbohydrate research 20030501

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