CAS 113826-06-5 | 2-Oxiranemethanol, 2-(4-methylbenzenesulfonate), (2R)- | CAS Number 113826-06-5

200,000+ products from a single source!

sales@angenechem.com

Product Categories

Home > Other Building Blocks > 113826-06-5

113826-06-5 | 2-Oxiranemethanol, 2-(4-methylbenzenesulfonate), (2R)-

CAS No: 113826-06-5 Catalog No: AG0009TL MDL No:MFCD00010834

Product Description

Catalog Number:

AG0009TL

Chemical Name:

2-Oxiranemethanol, 2-(4-methylbenzenesulfonate), (2R)-

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:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

228.046g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

228.262g/mol

Monoisotopic Mass:

228.046g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

64.3A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

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