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Home Other Building Blocks (2R)-(-)-Glycidyl tosylate

(2R)-(-)-Glycidyl tosylate

CAS No.:
113826-06-5
Catalog Number:
AG0009TL
Molecular Formula:
C10H12O4S
Molecular Weight:
228.2649
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%(GC)
In Stock USA
United States
$41
- +
25g
97%
In Stock USA
United States
$44
- +
100g
97%
In Stock USA
United States
$119
- +
500g
97%
In Stock USA
United States
$475
- +
Product Description
Catalog Number:
AG0009TL
Chemical Name:
(2R)-(-)-Glycidyl tosylate
CAS Number:
113826-06-5
Molecular Formula:
C10H12O4S
Molecular Weight:
228.2649
MDL Number:
MFCD00010834
IUPAC Name:
[(2R)-oxiran-2-yl]methyl 4-methylbenzenesulfonate
InChI:
InChI=1S/C10H12O4S/c1-8-2-4-10(5-3-8)15(11,12)14-7-9-6-13-9/h2-5,9H,6-7H2,1H3/t9-/m1/s1
InChI Key:
NOQXXYIGRPAZJC-SECBINFHSA-N
SMILES:
Cc1ccc(cc1)S(=O)(=O)OC[C@@H]1OC1
UNII:
62V982IWII
Properties
Complexity:
298  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0
Exact Mass:
228.046g/mol
Formal Charge:
0
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
228.262g/mol
Monoisotopic Mass:
228.046g/mol
Rotatable Bond Count:
4  
Topological Polar Surface Area:
64.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.1  
Literature
Title Journal
Enantiomeric separation of glycidyl tosylate by CE: application to the study of catalytic asymmetric epoxidation of allyl alcohol. Electrophoresis 20081101
Development and validation of a chiral HPLC method for rapid screening of allylic alcohol asymmetric epoxidation processes. Analytica chimica acta 20080616
Ru-catalyzed alkene-alkyne coupling. Total synthesis of amphidinolide P. Journal of the American Chemical Society 20051221
Synthesis of calix[4]arene and porphyrin tethering four chiral five-membered cyclic carbonates. Enantiomer 20020101
Properties