(2-Methyloxiran-2-yl)methyl (R)-4-Nitrobenzenesulfonate - CAS 683276-64-4
Catalog: |
BB033529 |
Product Name: |
(2-Methyloxiran-2-yl)methyl (R)-4-Nitrobenzenesulfonate |
CAS: |
683276-64-4 |
Synonyms: |
4-nitrobenzenesulfonic acid [(2R)-2-methyl-2-oxiranyl]methyl ester; [(2R)-2-methyloxiran-2-yl]methyl 4-nitrobenzenesulfonate |
IUPAC Name: | [(2R)-2-methyloxiran-2-yl]methyl 4-nitrobenzenesulfonate |
Description: | (2-Methyloxiran-2-yl)methyl (R)-4-Nitrobenzenesulfonate (CAS# 683276-64-4 ) is a useful research chemical. |
Molecular Weight: | 273.26 |
Molecular Formula: | C10H11NO6S |
Canonical SMILES: | CC1(CO1)COS(=O)(=O)C2=CC=C(C=C2)[N+](=O)[O-] |
InChI: | InChI=1S/C10H11NO6S/c1-10(6-16-10)7-17-18(14,15)9-4-2-8(3-5-9)11(12)13/h2-5H,6-7H2,1H3/t10-/m1/s1 |
InChI Key: | NXRMOVSGORLBCA-SNVBAGLBSA-N |
LogP: | 2.69300 |
Publication Number | Title | Priority Date |
WO-2020223267-A1 | (r)-(2-methyloxiran-2-yl)methyl 4-bromobenzenesulfonate | 20190501 |
US-2012302757-A1 | Synthetic intermediate of oxazole compound and method for producing the same | 20100129 |
US-8598358-B2 | Synthetic intermediate of oxazole compound and method for producing the same | 20100129 |
WO-2011093529-A1 | Synthetic intermediate of oxazole compound and method for producing the same | 20100129 |
US-8344148-B2 | Epoxy compound and method for manufacturing the same | 20070508 |
Complexity: | 417 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 1 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 273.03070824 |
Formal Charge: | 0 |
Heavy Atom Count: | 18 |
Hydrogen Bond Acceptor Count: | 6 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 273.03070824 |
Rotatable Bond Count: | 4 |
Topological Polar Surface Area: | 110 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0.9 |
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