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Home Sulfos Glycidyl 4-toluenesulfonate

Glycidyl 4-toluenesulfonate

CAS No.:
6746-81-2
Catalog Number:
AG00FAGQ
Molecular Formula:
Molecular Weight:
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
In Stock USA
United States
$50
- +
5g
98%
In Stock USA
United States
$194
- +
25g
98%
In Stock USA
United States
$725
- +
Product Description
Catalog Number:
AG00FAGQ
Chemical Name:
Glycidyl 4-toluenesulfonate
CAS Number:
6746-81-2
MDL Number:
MFCD00066850
IUPAC Name:
oxiran-2-ylmethyl 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
InChI Key:
NOQXXYIGRPAZJC-UHFFFAOYSA-N
NSC Number:
143322
Properties
Complexity:
298  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
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:
1  
Undefined Bond Stereocenter Count:
0
XLogP3:
1.1  
Literature
Title Journal
Synthesis of ferrocenyl pyrazole-containing chiral aminoethanol derivatives and their inhibition against A549 and H322 lung cancer cells. European journal of medicinal chemistry 20120801
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
Solid-phase synthesis of oxazolidinones by cycloaddition of resin-bound epoxides with isocyanates. Journal of combinatorial chemistry 20030101
Properties